Canonical Allele Identifier: CA367396917
Gene: GCK HGNC NCBI

Linked Data

gnomAD v4: 7-44145188-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145188G>C , CM000669.2:g.44145188G>C GRCh38
NC_000007.13:g.44184787G>C , CM000669.1:g.44184787G>C GRCh37
NC_000007.12:g.44151312G>C NCBI36
NG_008847.1:g.49236C>G
NG_008847.2:g.57983C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1344C>G ENSP00000379142.4:n.*1344C>G
ENST00000616242.5:c.*466C>G ENSP00000482149.2:n.*466C>G
ENST00000683378.1:n.572C>G
ENST00000336642.9:c.380C>G ENSP00000338009.5:p.Ala127Gly
ENST00000345378.7:c.1349C>G ENSP00000223366.2:p.Ala450Gly
ENST00000403799.8:c.1346C>G MANE Select ENSP00000384247.3:p.Ala449Gly
ENST00000671824.1:c.1409C>G ENSP00000500264.1:p.Ala470Gly
ENST00000672743.1:n.358C>G
ENST00000673284.1:c.1346C>G ENSP00000499852.1:p.Ala449Gly
ENST00000336642.8:c.398C>G ENSP00000338009.4:p.Ala133Gly
ENST00000345378.6:c.1349C>G ENSP00000223366.2:p.Ala450Gly
ENST00000395796.7:c.1343C>G ENSP00000379142.3:p.Ala448Gly
ENST00000403799.7:c.1346C>G ENSP00000384247.3:p.Ala449Gly
ENST00000437084.1:c.1295C>G ENSP00000402840.1:p.Ala432Gly
ENST00000459642.1:n.726C>G
ENST00000616242.4:c.1343C>G ENSP00000482149.1:p.Ala448Gly
NM_000162.3:c.1346C>G NP_000153.1:p.Ala449Gly
NM_033507.1:c.1349C>G NP_277042.1:p.Ala450Gly
NM_033508.1:c.1343C>G NP_277043.1:p.Ala448Gly
NM_000162.4:c.1346C>G NP_000153.1:p.Ala449Gly
NM_001354800.1:c.1346C>G NP_001341729.1:p.Ala449Gly
NM_001354801.1:c.335C>G NP_001341730.1:p.Ala112Gly
NM_001354802.1:c.206C>G NP_001341731.1:p.Ala69Gly
NM_001354803.1:c.380C>G NP_001341732.1:p.Ala127Gly
NM_033507.2:c.1349C>G NP_277042.1:p.Ala450Gly
NM_033508.2:c.1343C>G NP_277043.1:p.Ala448Gly
XM_024446707.1:c.206C>G XP_024302475.1:p.Ala69Gly
NM_000162.5:c.1346C>G MANE Select NP_000153.1:p.Ala449Gly
NM_033507.3:c.1349C>G NP_277042.1:p.Ala450Gly
NM_033508.3:c.1343C>G NP_277043.1:p.Ala448Gly
NM_001354803.2:c.380C>G NP_001341732.1:p.Ala127Gly