Canonical Allele Identifier: CA367398867
Gene: GCK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145629A>G , CM000669.2:g.44145629A>G GRCh38
NC_000007.13:g.44185228A>G , CM000669.1:g.44185228A>G GRCh37
NC_000007.12:g.44151753A>G NCBI36
NG_008847.1:g.48795T>C
NG_008847.2:g.57542T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1119T>C ENSP00000379142.4:n.*1119T>C
ENST00000616242.5:c.*241T>C ENSP00000482149.2:n.*241T>C
ENST00000683378.1:n.347T>C
ENST00000336642.9:c.155T>C ENSP00000338009.5:p.Val52Ala
ENST00000345378.7:c.1124T>C ENSP00000223366.2:p.Val375Ala
ENST00000403799.8:c.1121T>C MANE Select ENSP00000384247.3:p.Val374Ala
ENST00000671824.1:c.1184T>C ENSP00000500264.1:p.Val395Ala
ENST00000672743.1:n.133T>C
ENST00000673284.1:c.1121T>C ENSP00000499852.1:p.Val374Ala
ENST00000336642.8:c.173T>C ENSP00000338009.4:p.Val58Ala
ENST00000345378.6:c.1124T>C ENSP00000223366.2:p.Val375Ala
ENST00000395796.7:c.1118T>C ENSP00000379142.3:p.Val373Ala
ENST00000403799.7:c.1121T>C ENSP00000384247.3:p.Val374Ala
ENST00000437084.1:c.1070T>C ENSP00000402840.1:p.Val357Ala
ENST00000459642.1:n.501T>C
ENST00000616242.4:c.1118T>C ENSP00000482149.1:p.Val373Ala
NM_000162.3:c.1121T>C NP_000153.1:p.Val374Ala
NM_033507.1:c.1124T>C NP_277042.1:p.Val375Ala
NM_033508.1:c.1118T>C NP_277043.1:p.Val373Ala
NM_000162.4:c.1121T>C NP_000153.1:p.Val374Ala
NM_001354800.1:c.1121T>C NP_001341729.1:p.Val374Ala
NM_001354801.1:c.110T>C NP_001341730.1:p.Val37Ala
NM_001354802.1:c.-20T>C NP_001341731.1:n.-20T>C
NM_001354803.1:c.155T>C NP_001341732.1:p.Val52Ala
NM_033507.2:c.1124T>C NP_277042.1:p.Val375Ala
NM_033508.2:c.1118T>C NP_277043.1:p.Val373Ala
XM_024446707.1:c.-20T>C XP_024302475.1:n.-20T>C
NM_000162.5:c.1121T>C MANE Select NP_000153.1:p.Val374Ala
NM_033507.3:c.1124T>C NP_277042.1:p.Val375Ala
NM_033508.3:c.1118T>C NP_277043.1:p.Val373Ala
NM_001354803.2:c.155T>C NP_001341732.1:p.Val52Ala