Canonical Allele Identifier: CA4239412
Gene: GCK HGNC NCBI

Linked Data

dbSNP Id: rs767892728
gnomAD v2: 7-44185128-G-T
gnomAD v3: 7-44145529-G-T
gnomAD v4: 7-44145529-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145529G>T , CM000669.2:g.44145529G>T GRCh38
NC_000007.13:g.44185128G>T , CM000669.1:g.44185128G>T GRCh37
NC_000007.12:g.44151653G>T NCBI36
NG_008847.1:g.48895C>A
NG_008847.2:g.57642C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000395796.8:c.*1219C>A ENSP00000379142.4:n.*1219C>A
ENST00000616242.5:c.*341C>A ENSP00000482149.2:n.*341C>A
ENST00000683378.1:n.447C>A
ENST00000336642.9:c.255C>A ENSP00000338009.5:p.Gly85=
ENST00000345378.7:c.1224C>A ENSP00000223366.2:p.Gly408=
ENST00000403799.8:c.1221C>A MANE Select ENSP00000384247.3:p.Gly407=
ENST00000671824.1:c.1284C>A ENSP00000500264.1:p.Gly428=
ENST00000672743.1:n.233C>A
ENST00000673284.1:c.1221C>A ENSP00000499852.1:p.Gly407=
ENST00000336642.8:c.273C>A ENSP00000338009.4:p.Gly91=
ENST00000345378.6:c.1224C>A ENSP00000223366.2:p.Gly408=
ENST00000395796.7:c.1218C>A ENSP00000379142.3:p.Gly406=
ENST00000403799.7:c.1221C>A ENSP00000384247.3:p.Gly407=
ENST00000437084.1:c.1170C>A ENSP00000402840.1:p.Gly390=
ENST00000459642.1:n.601C>A
ENST00000616242.4:c.1218C>A ENSP00000482149.1:p.Gly406=
NM_000162.3:c.1221C>A NP_000153.1:p.Gly407=
NM_033507.1:c.1224C>A NP_277042.1:p.Gly408=
NM_033508.1:c.1218C>A NP_277043.1:p.Gly406=
NM_000162.4:c.1221C>A NP_000153.1:p.Gly407=
NM_001354800.1:c.1221C>A NP_001341729.1:p.Gly407=
NM_001354801.1:c.210C>A NP_001341730.1:p.Gly70=
NM_001354802.1:c.81C>A NP_001341731.1:p.Gly27=
NM_001354803.1:c.255C>A NP_001341732.1:p.Gly85=
NM_033507.2:c.1224C>A NP_277042.1:p.Gly408=
NM_033508.2:c.1218C>A NP_277043.1:p.Gly406=
XM_024446707.1:c.81C>A XP_024302475.1:p.Gly27=
NM_000162.5:c.1221C>A MANE Select NP_000153.1:p.Gly407=
NM_033507.3:c.1224C>A NP_277042.1:p.Gly408=
NM_033508.3:c.1218C>A NP_277043.1:p.Gly406=
NM_001354803.2:c.255C>A NP_001341732.1:p.Gly85=