Canonical Allele Identifier: CA1703612851
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145515A= , CM000669.2:g.44145515A= GRCh38
NC_000007.13:g.44185114A= , CM000669.1:g.44185114A= GRCh37
NC_000007.12:g.44151639A= NCBI36
NG_008847.1:g.48909T=
NG_008847.2:g.57656T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1233T= ENSP00000379142.4:n.*1233T=
ENST00000616242.5:c.*355T= ENSP00000482149.2:n.*355T=
ENST00000683378.1:n.461T=
ENST00000336642.9:c.269T= ENSP00000338009.5:p.Val90=
ENST00000345378.7:c.1238T= ENSP00000223366.2:p.Val413=
ENST00000403799.8:c.1235T= MANE Select ENSP00000384247.3:p.Val412=
ENST00000671824.1:c.1298T= ENSP00000500264.1:p.Val433=
ENST00000672743.1:n.247T=
ENST00000673284.1:c.1235T= ENSP00000499852.1:p.Val412=
ENST00000336642.8:c.287T= ENSP00000338009.4:p.Val96=
ENST00000345378.6:c.1238T= ENSP00000223366.2:p.Val413=
ENST00000395796.7:c.1232T= ENSP00000379142.3:p.Val411=
ENST00000403799.7:c.1235T= ENSP00000384247.3:p.Val412=
ENST00000437084.1:c.1184T= ENSP00000402840.1:p.Val395=
ENST00000459642.1:n.615T=
ENST00000616242.4:c.1232T= ENSP00000482149.1:p.Val411=
NM_000162.3:c.1235T= NP_000153.1:p.Val412=
NM_033507.1:c.1238T= NP_277042.1:p.Val413=
NM_033508.1:c.1232T= NP_277043.1:p.Val411=
NM_000162.4:c.1235T= NP_000153.1:p.Val412=
NM_001354800.1:c.1235T= NP_001341729.1:p.Val412=
NM_001354801.1:c.224T= NP_001341730.1:p.Val75=
NM_001354802.1:c.95T= NP_001341731.1:p.Val32=
NM_001354803.1:c.269T= NP_001341732.1:p.Val90=
NM_033507.2:c.1238T= NP_277042.1:p.Val413=
NM_033508.2:c.1232T= NP_277043.1:p.Val411=
XM_024446707.1:c.95T= XP_024302475.1:p.Val32=
NM_000162.5:c.1235T= MANE Select NP_000153.1:p.Val412=
NM_033507.3:c.1238T= NP_277042.1:p.Val413=
NM_033508.3:c.1232T= NP_277043.1:p.Val411=
NM_001354803.2:c.269T= NP_001341732.1:p.Val90=