Canonical Allele Identifier: CA1703653831

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44189382C= , CM000669.2:g.44189382C=	GRCh38
NC_000007.13:g.44228981C= , CM000669.1:g.44228981C=	GRCh37
NC_000007.12:g.44195506C=	NCBI36
NG_008847.1:g.5042G=
NG_008847.2:g.13789G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000616242.5:c.-429G=	ENSP00000482149.2:n.-429G=
ENST00000682635.1:n.58G=
ENST00000403799.8:c.-429G= MANE Select	ENSP00000384247.3:n.-429G=
ENST00000671824.1:c.-429G=	ENSP00000500264.1:n.-429G=
ENST00000673284.1:c.-429G=	ENSP00000499852.1:n.-429G=
ENST00000403799.7:c.-429G=	ENSP00000384247.3:n.-429G=
ENST00000476008.1:n.480+8309G=
NM_000162.3:c.-429G=	NP_000153.1:n.-429G=
NM_000162.4:c.-429G=	NP_000153.1:n.-429G=
NM_001354800.1:c.-429G=	NP_001341729.1:n.-429G=
NM_000162.5:c.-429G= MANE Select	NP_000153.1:n.-429G=