Canonical Allele Identifier: CA1703635861
Gene: GCK HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44149784G= , CM000669.2:g.44149784G= GRCh38
NC_000007.13:g.44189383G= , CM000669.1:g.44189383G= GRCh37
NC_000007.12:g.44155908G= NCBI36
NG_008847.1:g.44640C=
NG_008847.2:g.53387C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*653C= ENSP00000379142.4:n.*653C=
ENST00000616242.5:c.655C= ENSP00000482149.2:p.Gln219=
ENST00000682635.1:n.1141C=
ENST00000345378.7:c.658C= ENSP00000223366.2:p.Gln220=
ENST00000403799.8:c.655C= MANE Select ENSP00000384247.3:p.Gln219=
ENST00000671824.1:c.655C= ENSP00000500264.1:p.Gln219=
ENST00000673284.1:c.655C= ENSP00000499852.1:p.Gln219=
ENST00000345378.6:c.658C= ENSP00000223366.2:p.Gln220=
ENST00000395796.7:c.652C= ENSP00000379142.3:p.Gln218=
ENST00000403799.7:c.655C= ENSP00000384247.3:p.Gln219=
ENST00000437084.1:c.604C= ENSP00000402840.1:p.Gln202=
ENST00000616242.4:c.652C= ENSP00000482149.1:p.Gln218=
NM_000162.3:c.655C= NP_000153.1:p.Gln219=
NM_033507.1:c.658C= NP_277042.1:p.Gln220=
NM_033508.1:c.652C= NP_277043.1:p.Gln218=
NM_000162.4:c.655C= NP_000153.1:p.Gln219=
NM_001354800.1:c.655C= NP_001341729.1:p.Gln219=
NM_033507.2:c.658C= NP_277042.1:p.Gln220=
NM_033508.2:c.652C= NP_277043.1:p.Gln218=
NM_000162.5:c.655C= MANE Select NP_000153.1:p.Gln219=
NM_033507.3:c.658C= NP_277042.1:p.Gln220=
NM_033508.3:c.652C= NP_277043.1:p.Gln218=
Search 100 bp 5'
Search 100 bp 3'