Canonical Allele Identifier: CA1703612963
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145708T= , CM000669.2:g.44145708T= GRCh38
NC_000007.13:g.44185307T= , CM000669.1:g.44185307T= GRCh37
NC_000007.12:g.44151832T= NCBI36
NG_008847.1:g.48716A=
NG_008847.2:g.57463A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1040A= ENSP00000379142.4:n.*1040A=
ENST00000616242.5:c.*162A= ENSP00000482149.2:n.*162A=
ENST00000683378.1:n.268A=
ENST00000336642.9:c.76A= ENSP00000338009.5:p.Ile26=
ENST00000345378.7:c.1045A= ENSP00000223366.2:p.Ile349=
ENST00000403799.8:c.1042A= MANE Select ENSP00000384247.3:p.Ile348=
ENST00000671824.1:c.1105A= ENSP00000500264.1:p.Ile369=
ENST00000672743.1:n.54A=
ENST00000673284.1:c.1042A= ENSP00000499852.1:p.Ile348=
ENST00000336642.8:c.94A= ENSP00000338009.4:p.Ile32=
ENST00000345378.6:c.1045A= ENSP00000223366.2:p.Ile349=
ENST00000395796.7:c.1039A= ENSP00000379142.3:p.Ile347=
ENST00000403799.7:c.1042A= ENSP00000384247.3:p.Ile348=
ENST00000437084.1:c.991A= ENSP00000402840.1:p.Ile331=
ENST00000459642.1:n.422A=
ENST00000473353.1:n.340A=
ENST00000616242.4:c.1039A= ENSP00000482149.1:p.Ile347=
NM_000162.3:c.1042A= NP_000153.1:p.Ile348=
NM_033507.1:c.1045A= NP_277042.1:p.Ile349=
NM_033508.1:c.1039A= NP_277043.1:p.Ile347=
NM_000162.4:c.1042A= NP_000153.1:p.Ile348=
NM_001354800.1:c.1042A= NP_001341729.1:p.Ile348=
NM_001354801.1:c.31A= NP_001341730.1:p.Ile11=
NM_001354802.1:c.-99A= NP_001341731.1:n.-99A=
NM_001354803.1:c.76A= NP_001341732.1:p.Ile26=
NM_033507.2:c.1045A= NP_277042.1:p.Ile349=
NM_033508.2:c.1039A= NP_277043.1:p.Ile347=
XM_024446707.1:c.-99A= XP_024302475.1:n.-99A=
NM_000162.5:c.1042A= MANE Select NP_000153.1:p.Ile348=
NM_033507.3:c.1045A= NP_277042.1:p.Ile349=
NM_033508.3:c.1039A= NP_277043.1:p.Ile347=
NM_001354803.2:c.76A= NP_001341732.1:p.Ile26=