Canonical Allele Identifier: CA367401119

Gene: GCK

Linked Data

• MyVariant Identifiers: chr7:g.44189361A>T (hg19) ; chr7:g.44149762A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44149762A>T , CM000669.2:g.44149762A>T	GRCh38
NC_000007.13:g.44189361A>T , CM000669.1:g.44189361A>T	GRCh37
NC_000007.12:g.44155886A>T	NCBI36
NG_008847.1:g.44662T>A
NG_008847.2:g.53409T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000395796.8:c.*675T>A	ENSP00000379142.4:n.*675T>A
ENST00000616242.5:c.677T>A	ENSP00000482149.2:p.Val226Glu
ENST00000682635.1:n.1163T>A
ENST00000345378.7:c.680T>A	ENSP00000223366.2:p.Val227Glu
ENST00000403799.8:c.677T>A MANE Select	ENSP00000384247.3:p.Val226Glu
ENST00000671824.1:c.677T>A	ENSP00000500264.1:p.Val226Glu
ENST00000673284.1:c.677T>A	ENSP00000499852.1:p.Val226Glu
ENST00000345378.6:c.680T>A	ENSP00000223366.2:p.Val227Glu
ENST00000395796.7:c.674T>A	ENSP00000379142.3:p.Val225Glu
ENST00000403799.7:c.677T>A	ENSP00000384247.3:p.Val226Glu
ENST00000437084.1:c.626T>A	ENSP00000402840.1:p.Val209Glu
ENST00000616242.4:c.674T>A	ENSP00000482149.1:p.Val225Glu
NM_000162.3:c.677T>A	NP_000153.1:p.Val226Glu
NM_033507.1:c.680T>A	NP_277042.1:p.Val227Glu
NM_033508.1:c.674T>A	NP_277043.1:p.Val225Glu
XR_927223.1:n.277A>T
NM_000162.4:c.677T>A	NP_000153.1:p.Val226Glu
NM_001354800.1:c.677T>A	NP_001341729.1:p.Val226Glu
NM_033507.2:c.680T>A	NP_277042.1:p.Val227Glu
NM_033508.2:c.674T>A	NP_277043.1:p.Val225Glu
XR_927223.2:n.277A>T
NM_000162.5:c.677T>A MANE Select	NP_000153.1:p.Val226Glu
NM_033507.3:c.680T>A	NP_277042.1:p.Val227Glu
NM_033508.3:c.674T>A	NP_277043.1:p.Val225Glu