Canonical Allele Identifier: CA2775231444
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44151176_44151181del , CM000669.2:g.44151176_44151181del GRCh38
NC_000007.13:g.44190775_44190780del , CM000669.1:g.44190775_44190780del GRCh37
NC_000007.12:g.44157300_44157305del NCBI36
NG_008847.1:g.43244_43249del
NG_008847.2:g.51991_51996del

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*362-105_*362-100del ENSP00000379142.4:n.*362-105_*362-100del
ENST00000616242.5:c.364-105_364-100del ENSP00000482149.2:n.364-105_364-100del
ENST00000682635.1:n.850-105_850-100del
ENST00000345378.7:c.367-105_367-100del ENSP00000223366.2:n.367-105_367-100del
ENST00000403799.8:c.364-105_364-100del MANE Select ENSP00000384247.3:n.364-105_364-100del
ENST00000671824.1:c.364-105_364-100del ENSP00000500264.1:n.364-105_364-100del
ENST00000673284.1:c.364-105_364-100del ENSP00000499852.1:n.364-105_364-100del
ENST00000345378.6:c.367-105_367-100del ENSP00000223366.2:n.367-105_367-100del
ENST00000395796.7:c.361-105_361-100del ENSP00000379142.3:n.361-105_361-100del
ENST00000403799.7:c.364-105_364-100del ENSP00000384247.3:n.364-105_364-100del
ENST00000437084.1:c.364-156_364-151del ENSP00000402840.1:n.364-156_364-151del
ENST00000616242.4:c.361-105_361-100del ENSP00000482149.1:n.361-105_361-100del
NM_000162.3:c.364-105_364-100del NP_000153.1:n.364-105_364-100del
NM_033507.1:c.367-105_367-100del NP_277042.1:n.367-105_367-100del
NM_033508.1:c.361-105_361-100del NP_277043.1:n.361-105_361-100del
NM_000162.4:c.364-105_364-100del NP_000153.1:n.364-105_364-100del
NM_001354800.1:c.364-105_364-100del NP_001341729.1:n.364-105_364-100del
NM_033507.2:c.367-105_367-100del NP_277042.1:n.367-105_367-100del
NM_033508.2:c.361-105_361-100del NP_277043.1:n.361-105_361-100del
NM_000162.5:c.364-105_364-100del MANE Select NP_000153.1:n.364-105_364-100del
NM_033507.3:c.367-105_367-100del NP_277042.1:n.367-105_367-100del
NM_033508.3:c.361-105_361-100del NP_277043.1:n.361-105_361-100del