Canonical Allele Identifier: CA2536355917
Gene: GCK HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44144928_44144929insTCACACTCCGGCTGAACATCGCC , CM000669.2:g.44144928_44144929insTCACACTCCGGCTGAACATCGCC GRCh38
NC_000007.13:g.44184527_44184528insTCACACTCCGGCTGAACATCGCC , CM000669.1:g.44184527_44184528insTCACACTCCGGCTGAACATCGCC GRCh37
NC_000007.12:g.44151052_44151053insTCACACTCCGGCTGAACATCGCC NCBI36
NG_008847.1:g.49496_49497insGCGATGTTCAGCCGGAGTGTGAG
NG_008847.2:g.58243_58244insGCGATGTTCAGCCGGAGTGTGAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1604_*1605insGCGATGTTCAGCCGGAGTGTGAG ENSP00000379142.4:n.*1604_*1605insGCGATGTTCAGCCGGAGTGTGAG
ENST00000616242.5:c.*726_*727insGCGATGTTCAGCCGGAGTGTGAG ENSP00000482149.2:n.*726_*727insGCGATGTTCAGCCGGAGTGTGAG
ENST00000683378.1:n.832_833insGCGATGTTCAGCCGGAGTGTGAG
ENST00000336642.9:c.*208_*209insGCGATGTTCAGCCGGAGTGTGAG ENSP00000338009.5:n.*208_*209insGCGATGTTCAGCCGGAGTGTGAG
ENST00000345378.7:c.*208_*209insGCGATGTTCAGCCGGAGTGTGAG ENSP00000223366.2:n.*208_*209insGCGATGTTCAGCCGGAGTGTGAG
ENST00000403799.8:c.*208_*209insGCGATGTTCAGCCGGAGTGTGAG MANE Select ENSP00000384247.3:n.*208_*209insGCGATGTTCAGCCGGAGTGTGAG
ENST00000671824.1:c.*208_*209insGCGATGTTCAGCCGGAGTGTGAG ENSP00000500264.1:n.*208_*209insGCGATGTTCAGCCGGAGTGTGAG
ENST00000672743.1:n.381+237_381+238insGCGATGTTCAGCCGGAGTGTGAG
ENST00000673284.1:c.1369+237_1369+238insGCGATGTTCAGCCGGAGTGTGAG ENSP00000499852.1:n.1369+237_1369+238insGCGATGTTCAGCCGGAGTGTG...
ENST00000336642.8:c.658_659insGCGATGTTCAGCCGGAGTGTGAG ENSP00000338009.4:n.658_659insGCGATGTTCAGCCGGAGTGTGAG
ENST00000345378.6:c.*208_*209insGCGATGTTCAGCCGGAGTGTGAG ENSP00000223366.2:n.*208_*209insGCGATGTTCAGCCGGAGTGTGAG
ENST00000395796.7:c.*208_*209insGCGATGTTCAGCCGGAGTGTGAG ENSP00000379142.3:n.*208_*209insGCGATGTTCAGCCGGAGTGTGAG
ENST00000403799.7:c.*208_*209insGCGATGTTCAGCCGGAGTGTGAG ENSP00000384247.3:n.*208_*209insGCGATGTTCAGCCGGAGTGTGAG
ENST00000459642.1:n.986_987insGCGATGTTCAGCCGGAGTGTGAG
ENST00000616242.4:c.1603_1604insGCGATGTTCAGCCGGAGTGTGAG ENSP00000482149.1:n.1603_1604insGCGATGTTCAGCCGGAGTGTGAG
NM_000162.3:c.*208_*209insGCGATGTTCAGCCGGAGTGTGAG NP_000153.1:n.*208_*209insGCGATGTTCAGCCGGAGTGTGAG
NM_033507.1:c.*208_*209insGCGATGTTCAGCCGGAGTGTGAG NP_277042.1:n.*208_*209insGCGATGTTCAGCCGGAGTGTGAG
NM_033508.1:c.*208_*209insGCGATGTTCAGCCGGAGTGTGAG NP_277043.1:n.*208_*209insGCGATGTTCAGCCGGAGTGTGAG
NM_000162.4:c.*208_*209insGCGATGTTCAGCCGGAGTGTGAG NP_000153.1:n.*208_*209insGCGATGTTCAGCCGGAGTGTGAG
NM_001354800.1:c.1369+237_1369+238insGCGATGTTCAGCCGGAGTGTGAG NP_001341729.1:n.1369+237_1369+238insGCGATGTTCAGCCGGAGTGTGAG
NM_001354801.1:c.*208_*209insGCGATGTTCAGCCGGAGTGTGAG NP_001341730.1:n.*208_*209insGCGATGTTCAGCCGGAGTGTGAG
NM_001354802.1:c.229+237_229+238insGCGATGTTCAGCCGGAGTGTGAG NP_001341731.1:n.229+237_229+238insGCGATGTTCAGCCGGAGTGTGAG
NM_001354803.1:c.*208_*209insGCGATGTTCAGCCGGAGTGTGAG NP_001341732.1:n.*208_*209insGCGATGTTCAGCCGGAGTGTGAG
NM_033507.2:c.*208_*209insGCGATGTTCAGCCGGAGTGTGAG NP_277042.1:n.*208_*209insGCGATGTTCAGCCGGAGTGTGAG
NM_033508.2:c.*208_*209insGCGATGTTCAGCCGGAGTGTGAG NP_277043.1:n.*208_*209insGCGATGTTCAGCCGGAGTGTGAG
XM_024446707.1:c.*208_*209insGCGATGTTCAGCCGGAGTGTGAG XP_024302475.1:n.*208_*209insGCGATGTTCAGCCGGAGTGTGAG
NM_000162.5:c.*208_*209insGCGATGTTCAGCCGGAGTGTGAG MANE Select NP_000153.1:n.*208_*209insGCGATGTTCAGCCGGAGTGTGAG
NM_033507.3:c.*208_*209insGCGATGTTCAGCCGGAGTGTGAG NP_277042.1:n.*208_*209insGCGATGTTCAGCCGGAGTGTGAG
NM_033508.3:c.*208_*209insGCGATGTTCAGCCGGAGTGTGAG NP_277043.1:n.*208_*209insGCGATGTTCAGCCGGAGTGTGAG
NM_001354803.2:c.*208_*209insGCGATGTTCAGCCGGAGTGTGAG NP_001341732.1:n.*208_*209insGCGATGTTCAGCCGGAGTGTGAG
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