Canonical Allele Identifier: CA454608586

Gene: GCK

Linked Data

• MyVariant Identifiers: chr7:g.44187287G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44147688G>A , CM000669.2:g.44147688G>A	GRCh38
NC_000007.13:g.44187287G>A , CM000669.1:g.44187287G>A	GRCh37
NC_000007.12:g.44153812G>A	NCBI36
NG_008847.1:g.46736C>T
NG_008847.2:g.55483C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*823C>T	ENSP00000379142.4:n.*823C>T
ENST00000616242.5:c.825C>T	ENSP00000482149.2:p.Arg275=
ENST00000345378.7:c.828C>T	ENSP00000223366.2:p.Arg276=
ENST00000403799.8:c.825C>T MANE Select	ENSP00000384247.3:p.Arg275=
ENST00000671824.1:c.825C>T	ENSP00000500264.1:p.Arg275=
ENST00000673284.1:c.825C>T	ENSP00000499852.1:p.Arg275=
ENST00000345378.6:c.828C>T	ENSP00000223366.2:p.Arg276=
ENST00000395796.7:c.822C>T	ENSP00000379142.3:p.Arg274=
ENST00000403799.7:c.825C>T	ENSP00000384247.3:p.Arg275=
ENST00000437084.1:c.774C>T	ENSP00000402840.1:p.Arg258=
ENST00000616242.4:c.822C>T	ENSP00000482149.1:p.Arg274=
NM_000162.3:c.825C>T	NP_000153.1:p.Arg275=
NM_033507.1:c.828C>T	NP_277042.1:p.Arg276=
NM_033508.1:c.822C>T	NP_277043.1:p.Arg274=
XR_927223.1:n.22G>A
NM_000162.4:c.825C>T	NP_000153.1:p.Arg275=
NM_001354800.1:c.825C>T	NP_001341729.1:p.Arg275=
NM_033507.2:c.828C>T	NP_277042.1:p.Arg276=
NM_033508.2:c.822C>T	NP_277043.1:p.Arg274=
XR_927223.2:n.22G>A
NM_000162.5:c.825C>T MANE Select	NP_000153.1:p.Arg275=
NM_033507.3:c.828C>T	NP_277042.1:p.Arg276=
NM_033508.3:c.822C>T	NP_277043.1:p.Arg274=