Canonical Allele Identifier: CA1703612739
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145333A= , CM000669.2:g.44145333A= GRCh38
NC_000007.13:g.44184932A= , CM000669.1:g.44184932A= GRCh37
NC_000007.12:g.44151457A= NCBI36
NG_008847.1:g.49091T=
NG_008847.2:g.57838T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1252-53T= ENSP00000379142.4:n.*1252-53T=
ENST00000616242.5:c.*374-53T= ENSP00000482149.2:n.*374-53T=
ENST00000683378.1:n.480-53T=
ENST00000336642.9:c.288-53T= ENSP00000338009.5:n.288-53T=
ENST00000345378.7:c.1257-53T= ENSP00000223366.2:n.1257-53T=
ENST00000403799.8:c.1254-53T= MANE Select ENSP00000384247.3:n.1254-53T=
ENST00000671824.1:c.1317-53T= ENSP00000500264.1:n.1317-53T=
ENST00000672743.1:n.266-53T=
ENST00000673284.1:c.1254-53T= ENSP00000499852.1:n.1254-53T=
ENST00000336642.8:c.306-53T= ENSP00000338009.4:n.306-53T=
ENST00000345378.6:c.1257-53T= ENSP00000223366.2:n.1257-53T=
ENST00000395796.7:c.1251-53T= ENSP00000379142.3:n.1251-53T=
ENST00000403799.7:c.1254-53T= ENSP00000384247.3:n.1254-53T=
ENST00000437084.1:c.1203-53T= ENSP00000402840.1:n.1203-53T=
ENST00000459642.1:n.634-53T=
ENST00000616242.4:c.1251-53T= ENSP00000482149.1:n.1251-53T=
NM_000162.3:c.1254-53T= NP_000153.1:n.1254-53T=
NM_033507.1:c.1257-53T= NP_277042.1:n.1257-53T=
NM_033508.1:c.1251-53T= NP_277043.1:n.1251-53T=
NM_000162.4:c.1254-53T= NP_000153.1:n.1254-53T=
NM_001354800.1:c.1254-53T= NP_001341729.1:n.1254-53T=
NM_001354801.1:c.243-53T= NP_001341730.1:n.243-53T=
NM_001354802.1:c.114-53T= NP_001341731.1:n.114-53T=
NM_001354803.1:c.288-53T= NP_001341732.1:n.288-53T=
NM_033507.2:c.1257-53T= NP_277042.1:n.1257-53T=
NM_033508.2:c.1251-53T= NP_277043.1:n.1251-53T=
XM_024446707.1:c.114-53T= XP_024302475.1:n.114-53T=
NM_000162.5:c.1254-53T= MANE Select NP_000153.1:n.1254-53T=
NM_033507.3:c.1257-53T= NP_277042.1:n.1257-53T=
NM_033508.3:c.1251-53T= NP_277043.1:n.1251-53T=
NM_001354803.2:c.288-53T= NP_001341732.1:n.288-53T=