Canonical Allele Identifier: CA367396744
Gene: GCK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145144C>T , CM000669.2:g.44145144C>T GRCh38
NC_000007.13:g.44184743C>T , CM000669.1:g.44184743C>T GRCh37
NC_000007.12:g.44151268C>T NCBI36
NG_008847.1:g.49280G>A
NG_008847.2:g.58027G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1388G>A ENSP00000379142.4:n.*1388G>A
ENST00000616242.5:c.*510G>A ENSP00000482149.2:n.*510G>A
ENST00000683378.1:n.616G>A
ENST00000336642.9:c.424G>A ENSP00000338009.5:p.Gly142Ser
ENST00000345378.7:c.1393G>A ENSP00000223366.2:p.Gly465Ser
ENST00000403799.8:c.1390G>A MANE Select ENSP00000384247.3:p.Gly464Ser
ENST00000671824.1:c.1453G>A ENSP00000500264.1:p.Gly485Ser
ENST00000672743.1:n.381+21G>A
ENST00000673284.1:c.1369+21G>A ENSP00000499852.1:n.1369+21G>A
ENST00000336642.8:c.442G>A ENSP00000338009.4:p.Gly148Ser
ENST00000345378.6:c.1393G>A ENSP00000223366.2:p.Gly465Ser
ENST00000395796.7:c.1387G>A ENSP00000379142.3:p.Gly463Ser
ENST00000403799.7:c.1390G>A ENSP00000384247.3:p.Gly464Ser
ENST00000437084.1:c.1339G>A ENSP00000402840.1:p.Gly447Ser
ENST00000459642.1:n.770G>A
ENST00000616242.4:c.1387G>A ENSP00000482149.1:p.Gly463Ser
NM_000162.3:c.1390G>A NP_000153.1:p.Gly464Ser
NM_033507.1:c.1393G>A NP_277042.1:p.Gly465Ser
NM_033508.1:c.1387G>A NP_277043.1:p.Gly463Ser
NM_000162.4:c.1390G>A NP_000153.1:p.Gly464Ser
NM_001354800.1:c.1369+21G>A NP_001341729.1:n.1369+21G>A
NM_001354801.1:c.379G>A NP_001341730.1:p.Gly127Ser
NM_001354802.1:c.229+21G>A NP_001341731.1:n.229+21G>A
NM_001354803.1:c.424G>A NP_001341732.1:p.Gly142Ser
NM_033507.2:c.1393G>A NP_277042.1:p.Gly465Ser
NM_033508.2:c.1387G>A NP_277043.1:p.Gly463Ser
XM_024446707.1:c.250G>A XP_024302475.1:p.Gly84Ser
NM_000162.5:c.1390G>A MANE Select NP_000153.1:p.Gly464Ser
NM_033507.3:c.1393G>A NP_277042.1:p.Gly465Ser
NM_033508.3:c.1387G>A NP_277043.1:p.Gly463Ser
NM_001354803.2:c.424G>A NP_001341732.1:p.Gly142Ser