Canonical Allele Identifier: CA1703612895
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145591C= , CM000669.2:g.44145591C= GRCh38
NC_000007.13:g.44185190C= , CM000669.1:g.44185190C= GRCh37
NC_000007.12:g.44151715C= NCBI36
NG_008847.1:g.48833G=
NG_008847.2:g.57580G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1157G= ENSP00000379142.4:n.*1157G=
ENST00000616242.5:c.*279G= ENSP00000482149.2:n.*279G=
ENST00000683378.1:n.385G=
ENST00000336642.9:c.193G= ENSP00000338009.5:p.Ala65=
ENST00000345378.7:c.1162G= ENSP00000223366.2:p.Ala388=
ENST00000403799.8:c.1159G= MANE Select ENSP00000384247.3:p.Ala387=
ENST00000671824.1:c.1222G= ENSP00000500264.1:p.Ala408=
ENST00000672743.1:n.171G=
ENST00000673284.1:c.1159G= ENSP00000499852.1:p.Ala387=
ENST00000336642.8:c.211G= ENSP00000338009.4:p.Ala71=
ENST00000345378.6:c.1162G= ENSP00000223366.2:p.Ala388=
ENST00000395796.7:c.1156G= ENSP00000379142.3:p.Ala386=
ENST00000403799.7:c.1159G= ENSP00000384247.3:p.Ala387=
ENST00000437084.1:c.1108G= ENSP00000402840.1:p.Ala370=
ENST00000459642.1:n.539G=
ENST00000616242.4:c.1156G= ENSP00000482149.1:p.Ala386=
NM_000162.3:c.1159G= NP_000153.1:p.Ala387=
NM_033507.1:c.1162G= NP_277042.1:p.Ala388=
NM_033508.1:c.1156G= NP_277043.1:p.Ala386=
NM_000162.4:c.1159G= NP_000153.1:p.Ala387=
NM_001354800.1:c.1159G= NP_001341729.1:p.Ala387=
NM_001354801.1:c.148G= NP_001341730.1:p.Ala50=
NM_001354802.1:c.19G= NP_001341731.1:p.Ala7=
NM_001354803.1:c.193G= NP_001341732.1:p.Ala65=
NM_033507.2:c.1162G= NP_277042.1:p.Ala388=
NM_033508.2:c.1156G= NP_277043.1:p.Ala386=
XM_024446707.1:c.19G= XP_024302475.1:p.Ala7=
NM_000162.5:c.1159G= MANE Select NP_000153.1:p.Ala387=
NM_033507.3:c.1162G= NP_277042.1:p.Ala388=
NM_033508.3:c.1156G= NP_277043.1:p.Ala386=
NM_001354803.2:c.193G= NP_001341732.1:p.Ala65=