Canonical Allele Identifier: CA1703613522

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44146625A= , CM000669.2:g.44146625A=	GRCh38
NC_000007.13:g.44186224A= , CM000669.1:g.44186224A=	GRCh37
NC_000007.12:g.44152749A=	NCBI36
NG_008847.1:g.47799T=
NG_008847.2:g.56546T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*862-7T=	ENSP00000379142.4:n.*862-7T=
ENST00000616242.5:c.854-7T=	ENSP00000482149.2:n.854-7T=
ENST00000683378.1:n.83T=
ENST00000345378.7:c.867-7T=	ENSP00000223366.2:n.867-7T=
ENST00000403799.8:c.864-7T= MANE Select	ENSP00000384247.3:n.864-7T=
ENST00000671824.1:c.927-7T=	ENSP00000500264.1:n.927-7T=
ENST00000673284.1:c.864-7T=	ENSP00000499852.1:n.864-7T=
ENST00000345378.6:c.867-7T=	ENSP00000223366.2:n.867-7T=
ENST00000395796.7:c.861-7T=	ENSP00000379142.3:n.861-7T=
ENST00000403799.7:c.864-7T=	ENSP00000384247.3:n.864-7T=
ENST00000437084.1:c.813-7T=	ENSP00000402840.1:n.813-7T=
ENST00000473353.1:n.162-7T=
ENST00000616242.4:c.861-7T=	ENSP00000482149.1:n.861-7T=
NM_000162.3:c.864-7T=	NP_000153.1:n.864-7T=
NM_033507.1:c.867-7T=	NP_277042.1:n.867-7T=
NM_033508.1:c.861-7T=	NP_277043.1:n.861-7T=
NM_000162.4:c.864-7T=	NP_000153.1:n.864-7T=
NM_001354800.1:c.864-7T=	NP_001341729.1:n.864-7T=
NM_001354801.1:c.2T=	NP_001341730.1:p.Met1=
NM_033507.2:c.867-7T=	NP_277042.1:n.867-7T=
NM_033508.2:c.861-7T=	NP_277043.1:n.861-7T=
NM_000162.5:c.864-7T= MANE Select	NP_000153.1:n.864-7T=
NM_033507.3:c.867-7T=	NP_277042.1:n.867-7T=
NM_033508.3:c.861-7T=	NP_277043.1:n.861-7T=