Canonical Allele Identifier: CA1703612479
Gene: GCK HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44144835C= , CM000669.2:g.44144835C= GRCh38
NC_000007.13:g.44184434C= , CM000669.1:g.44184434C= GRCh37
NC_000007.12:g.44150959C= NCBI36
NG_008847.1:g.49589G=
NG_008847.2:g.58336G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1697G= ENSP00000379142.4:n.*1697G=
ENST00000616242.5:c.*819G= ENSP00000482149.2:n.*819G=
ENST00000683378.1:n.925G=
ENST00000336642.9:c.*301G= ENSP00000338009.5:n.*301G=
ENST00000345378.7:c.*301G= ENSP00000223366.2:n.*301G=
ENST00000403799.8:c.*301G= MANE Select ENSP00000384247.3:n.*301G=
ENST00000671824.1:c.*301G= ENSP00000500264.1:n.*301G=
ENST00000672743.1:n.381+330G=
ENST00000673284.1:c.1369+330G= ENSP00000499852.1:n.1369+330G=
ENST00000336642.8:c.751G= ENSP00000338009.4:n.751G=
ENST00000345378.6:c.*301G= ENSP00000223366.2:n.*301G=
ENST00000395796.7:c.*301G= ENSP00000379142.3:n.*301G=
ENST00000403799.7:c.*301G= ENSP00000384247.3:n.*301G=
ENST00000459642.1:n.1079G=
ENST00000616242.4:c.1696G= ENSP00000482149.1:n.1696G=
NM_000162.3:c.*301G= NP_000153.1:n.*301G=
NM_033507.1:c.*301G= NP_277042.1:n.*301G=
NM_033508.1:c.*301G= NP_277043.1:n.*301G=
NM_000162.4:c.*301G= NP_000153.1:n.*301G=
NM_001354800.1:c.1369+330G= NP_001341729.1:n.1369+330G=
NM_001354801.1:c.*301G= NP_001341730.1:n.*301G=
NM_001354802.1:c.229+330G= NP_001341731.1:n.229+330G=
NM_001354803.1:c.*301G= NP_001341732.1:n.*301G=
NM_033507.2:c.*301G= NP_277042.1:n.*301G=
NM_033508.2:c.*301G= NP_277043.1:n.*301G=
XM_024446707.1:c.*301G= XP_024302475.1:n.*301G=
NM_000162.5:c.*301G= MANE Select NP_000153.1:n.*301G=
NM_033507.3:c.*301G= NP_277042.1:n.*301G=
NM_033508.3:c.*301G= NP_277043.1:n.*301G=
NM_001354803.2:c.*301G= NP_001341732.1:n.*301G=
Search 100 bp 5'
Search 100 bp 3'