Canonical Allele Identifier: CA1703613486

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44146535A= , CM000669.2:g.44146535A=	GRCh38
NC_000007.13:g.44186134A= , CM000669.1:g.44186134A=	GRCh37
NC_000007.12:g.44152659A=	NCBI36
NG_008847.1:g.47889T=
NG_008847.2:g.56636T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*945T=	ENSP00000379142.4:n.*945T=
ENST00000616242.5:c.*67T=	ENSP00000482149.2:n.*67T=
ENST00000683378.1:n.173T=
ENST00000345378.7:c.950T=	ENSP00000223366.2:p.Phe317=
ENST00000403799.8:c.947T= MANE Select	ENSP00000384247.3:p.Phe316=
ENST00000671824.1:c.1010T=	ENSP00000500264.1:p.Phe337=
ENST00000673284.1:c.947T=	ENSP00000499852.1:p.Phe316=
ENST00000345378.6:c.950T=	ENSP00000223366.2:p.Phe317=
ENST00000395796.7:c.944T=	ENSP00000379142.3:p.Phe315=
ENST00000403799.7:c.947T=	ENSP00000384247.3:p.Phe316=
ENST00000437084.1:c.896T=	ENSP00000402840.1:p.Phe299=
ENST00000473353.1:n.245T=
ENST00000616242.4:c.944T=	ENSP00000482149.1:p.Phe315=
NM_000162.3:c.947T=	NP_000153.1:p.Phe316=
NM_033507.1:c.950T=	NP_277042.1:p.Phe317=
NM_033508.1:c.944T=	NP_277043.1:p.Phe315=
NM_000162.4:c.947T=	NP_000153.1:p.Phe316=
NM_001354800.1:c.947T=	NP_001341729.1:p.Phe316=
NM_001354801.1:c.8+84T=	NP_001341730.1:n.8+84T=
NM_033507.2:c.950T=	NP_277042.1:p.Phe317=
NM_033508.2:c.944T=	NP_277043.1:p.Phe315=
NM_000162.5:c.947T= MANE Select	NP_000153.1:p.Phe316=
NM_033507.3:c.950T=	NP_277042.1:p.Phe317=
NM_033508.3:c.944T=	NP_277043.1:p.Phe315=