Canonical Allele Identifier: CA1703612844
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145500G= , CM000669.2:g.44145500G= GRCh38
NC_000007.13:g.44185099G= , CM000669.1:g.44185099G= GRCh37
NC_000007.12:g.44151624G= NCBI36
NG_008847.1:g.48924C=
NG_008847.2:g.57671C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1248C= ENSP00000379142.4:n.*1248C=
ENST00000616242.5:c.*370C= ENSP00000482149.2:n.*370C=
ENST00000683378.1:n.476C=
ENST00000336642.9:c.284C= ENSP00000338009.5:p.Pro95=
ENST00000345378.7:c.1253C= ENSP00000223366.2:p.Pro418=
ENST00000403799.8:c.1250C= MANE Select ENSP00000384247.3:p.Pro417=
ENST00000671824.1:c.1313C= ENSP00000500264.1:p.Pro438=
ENST00000672743.1:n.262C=
ENST00000673284.1:c.1250C= ENSP00000499852.1:p.Pro417=
ENST00000336642.8:c.302C= ENSP00000338009.4:p.Pro101=
ENST00000345378.6:c.1253C= ENSP00000223366.2:p.Pro418=
ENST00000395796.7:c.1247C= ENSP00000379142.3:p.Pro416=
ENST00000403799.7:c.1250C= ENSP00000384247.3:p.Pro417=
ENST00000437084.1:c.1199C= ENSP00000402840.1:p.Pro400=
ENST00000459642.1:n.630C=
ENST00000616242.4:c.1247C= ENSP00000482149.1:p.Pro416=
NM_000162.3:c.1250C= NP_000153.1:p.Pro417=
NM_033507.1:c.1253C= NP_277042.1:p.Pro418=
NM_033508.1:c.1247C= NP_277043.1:p.Pro416=
NM_000162.4:c.1250C= NP_000153.1:p.Pro417=
NM_001354800.1:c.1250C= NP_001341729.1:p.Pro417=
NM_001354801.1:c.239C= NP_001341730.1:p.Pro80=
NM_001354802.1:c.110C= NP_001341731.1:p.Pro37=
NM_001354803.1:c.284C= NP_001341732.1:p.Pro95=
NM_033507.2:c.1253C= NP_277042.1:p.Pro418=
NM_033508.2:c.1247C= NP_277043.1:p.Pro416=
XM_024446707.1:c.110C= XP_024302475.1:p.Pro37=
NM_000162.5:c.1250C= MANE Select NP_000153.1:p.Pro417=
NM_033507.3:c.1253C= NP_277042.1:p.Pro418=
NM_033508.3:c.1247C= NP_277043.1:p.Pro416=
NM_001354803.2:c.284C= NP_001341732.1:p.Pro95=