Canonical Allele Identifier: CA1703653835

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44189394G= , CM000669.2:g.44189394G=	GRCh38
NC_000007.13:g.44228993G= , CM000669.1:g.44228993G=	GRCh37
NC_000007.12:g.44195518G=	NCBI36
NG_008847.1:g.5030C=
NG_008847.2:g.13777C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000616242.5:c.-441C=	ENSP00000482149.2:n.-441C=
ENST00000682635.1:n.46C=
ENST00000403799.8:c.-441C= MANE Select	ENSP00000384247.3:n.-441C=
ENST00000671824.1:c.-441C=	ENSP00000500264.1:n.-441C=
ENST00000673284.1:c.-441C=	ENSP00000499852.1:n.-441C=
ENST00000403799.7:c.-441C=	ENSP00000384247.3:n.-441C=
ENST00000476008.1:n.480+8297C=
NM_000162.3:c.-441C=	NP_000153.1:n.-441C=
NM_000162.4:c.-441C=	NP_000153.1:n.-441C=
NM_001354800.1:c.-441C=	NP_001341729.1:n.-441C=
NM_000162.5:c.-441C= MANE Select	NP_000153.1:n.-441C=