Canonical Allele Identifier: CA4239386
Gene: GCK HGNC NCBI

Linked Data

dbSNP Id: rs552762648
gnomAD v2: 7-44184851-G-A
gnomAD v3: 7-44145252-G-A
gnomAD v4: 7-44145252-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145252G>A , CM000669.2:g.44145252G>A GRCh38
NC_000007.13:g.44184851G>A , CM000669.1:g.44184851G>A GRCh37
NC_000007.12:g.44151376G>A NCBI36
NG_008847.1:g.49172C>T
NG_008847.2:g.57919C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1280C>T ENSP00000379142.4:n.*1280C>T
ENST00000616242.5:c.*402C>T ENSP00000482149.2:n.*402C>T
ENST00000683378.1:n.508C>T
ENST00000336642.9:c.316C>T ENSP00000338009.5:p.Arg106Cys
ENST00000345378.7:c.1285C>T ENSP00000223366.2:p.Arg429Cys
ENST00000403799.8:c.1282C>T MANE Select ENSP00000384247.3:p.Arg428Cys
ENST00000671824.1:c.1345C>T ENSP00000500264.1:p.Arg449Cys
ENST00000672743.1:n.294C>T
ENST00000673284.1:c.1282C>T ENSP00000499852.1:p.Arg428Cys
ENST00000336642.8:c.334C>T ENSP00000338009.4:p.Arg112Cys
ENST00000345378.6:c.1285C>T ENSP00000223366.2:p.Arg429Cys
ENST00000395796.7:c.1279C>T ENSP00000379142.3:p.Arg427Cys
ENST00000403799.7:c.1282C>T ENSP00000384247.3:p.Arg428Cys
ENST00000437084.1:c.1231C>T ENSP00000402840.1:p.Arg411Cys
ENST00000459642.1:n.662C>T
ENST00000616242.4:c.1279C>T ENSP00000482149.1:p.Arg427Cys
NM_000162.3:c.1282C>T NP_000153.1:p.Arg428Cys
NM_033507.1:c.1285C>T NP_277042.1:p.Arg429Cys
NM_033508.1:c.1279C>T NP_277043.1:p.Arg427Cys
NM_000162.4:c.1282C>T NP_000153.1:p.Arg428Cys
NM_001354800.1:c.1282C>T NP_001341729.1:p.Arg428Cys
NM_001354801.1:c.271C>T NP_001341730.1:p.Arg91Cys
NM_001354802.1:c.142C>T NP_001341731.1:p.Arg48Cys
NM_001354803.1:c.316C>T NP_001341732.1:p.Arg106Cys
NM_033507.2:c.1285C>T NP_277042.1:p.Arg429Cys
NM_033508.2:c.1279C>T NP_277043.1:p.Arg427Cys
XM_024446707.1:c.142C>T XP_024302475.1:p.Arg48Cys
NM_000162.5:c.1282C>T MANE Select NP_000153.1:p.Arg428Cys
NM_033507.3:c.1285C>T NP_277042.1:p.Arg429Cys
NM_033508.3:c.1279C>T NP_277043.1:p.Arg427Cys
NM_001354803.2:c.316C>T NP_001341732.1:p.Arg106Cys