Canonical Allele Identifier: CA1703635865

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44149798T= , CM000669.2:g.44149798T=	GRCh38
NC_000007.13:g.44189397T= , CM000669.1:g.44189397T=	GRCh37
NC_000007.12:g.44155922T=	NCBI36
NG_008847.1:g.44626A=
NG_008847.2:g.53373A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*639A=	ENSP00000379142.4:n.*639A=
ENST00000616242.5:c.641A=	ENSP00000482149.2:p.Tyr214=
ENST00000682635.1:n.1127A=
ENST00000345378.7:c.644A=	ENSP00000223366.2:p.Tyr215=
ENST00000403799.8:c.641A= MANE Select	ENSP00000384247.3:p.Tyr214=
ENST00000671824.1:c.641A=	ENSP00000500264.1:p.Tyr214=
ENST00000673284.1:c.641A=	ENSP00000499852.1:p.Tyr214=
ENST00000345378.6:c.644A=	ENSP00000223366.2:p.Tyr215=
ENST00000395796.7:c.638A=	ENSP00000379142.3:p.Tyr213=
ENST00000403799.7:c.641A=	ENSP00000384247.3:p.Tyr214=
ENST00000437084.1:c.590A=	ENSP00000402840.1:p.Tyr197=
ENST00000616242.4:c.638A=	ENSP00000482149.1:p.Tyr213=
NM_000162.3:c.641A=	NP_000153.1:p.Tyr214=
NM_033507.1:c.644A=	NP_277042.1:p.Tyr215=
NM_033508.1:c.638A=	NP_277043.1:p.Tyr213=
NM_000162.4:c.641A=	NP_000153.1:p.Tyr214=
NM_001354800.1:c.641A=	NP_001341729.1:p.Tyr214=
NM_033507.2:c.644A=	NP_277042.1:p.Tyr215=
NM_033508.2:c.638A=	NP_277043.1:p.Tyr213=
NM_000162.5:c.641A= MANE Select	NP_000153.1:p.Tyr214=
NM_033507.3:c.644A=	NP_277042.1:p.Tyr215=
NM_033508.3:c.638A=	NP_277043.1:p.Tyr213=