Canonical Allele Identifier: CA454610268

Gene: GCK

Linked Data

• MyVariant Identifiers: chr7:g.44191966C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44152367C>G , CM000669.2:g.44152367C>G	GRCh38
NC_000007.13:g.44191966C>G , CM000669.1:g.44191966C>G	GRCh37
NC_000007.12:g.44158491C>G	NCBI36
NG_008847.1:g.42057G>C
NG_008847.2:g.50804G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000395796.8:c.*265G>C	ENSP00000379142.4:n.*265G>C
ENST00000616242.5:c.267G>C	ENSP00000482149.2:p.Val89=
ENST00000682635.1:n.753G>C
ENST00000345378.7:c.270G>C	ENSP00000223366.2:p.Val90=
ENST00000403799.8:c.267G>C MANE Select	ENSP00000384247.3:p.Val89=
ENST00000671824.1:c.267G>C	ENSP00000500264.1:p.Val89=
ENST00000673284.1:c.267G>C	ENSP00000499852.1:p.Val89=
ENST00000345378.6:c.270G>C	ENSP00000223366.2:p.Val90=
ENST00000395796.7:c.264G>C	ENSP00000379142.3:p.Val88=
ENST00000403799.7:c.267G>C	ENSP00000384247.3:p.Val89=
ENST00000437084.1:c.267G>C	ENSP00000402840.1:p.Val89=
ENST00000616242.4:c.264G>C	ENSP00000482149.1:p.Val88=
NM_000162.3:c.267G>C	NP_000153.1:p.Val89=
NM_033507.1:c.270G>C	NP_277042.1:p.Val90=
NM_033508.1:c.264G>C	NP_277043.1:p.Val88=
NM_000162.4:c.267G>C	NP_000153.1:p.Val89=
NM_001354800.1:c.267G>C	NP_001341729.1:p.Val89=
NM_033507.2:c.270G>C	NP_277042.1:p.Val90=
NM_033508.2:c.264G>C	NP_277043.1:p.Val88=
NM_000162.5:c.267G>C MANE Select	NP_000153.1:p.Val89=
NM_033507.3:c.270G>C	NP_277042.1:p.Val90=
NM_033508.3:c.264G>C	NP_277043.1:p.Val88=