Canonical Allele Identifier: CA367401120

Gene: GCK

Linked Data

• ClinVar Variation Id: 2580858
• ClinVar RCV Id: RCV003330053
• MyVariant Identifiers: chr7:g.44189361A>C (hg19) ; chr7:g.44149762A>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000395796.8:c.*675T>G	ENSP00000379142.4:n.*675T>G
ENST00000616242.5:c.677T>G	ENSP00000482149.2:p.Val226Gly
ENST00000682635.1:n.1163T>G
ENST00000345378.7:c.680T>G	ENSP00000223366.2:p.Val227Gly
ENST00000403799.8:c.677T>G MANE Select	ENSP00000384247.3:p.Val226Gly
ENST00000671824.1:c.677T>G	ENSP00000500264.1:p.Val226Gly
ENST00000673284.1:c.677T>G	ENSP00000499852.1:p.Val226Gly
ENST00000345378.6:c.680T>G	ENSP00000223366.2:p.Val227Gly
ENST00000395796.7:c.674T>G	ENSP00000379142.3:p.Val225Gly
ENST00000403799.7:c.677T>G	ENSP00000384247.3:p.Val226Gly
ENST00000437084.1:c.626T>G	ENSP00000402840.1:p.Val209Gly
ENST00000616242.4:c.674T>G	ENSP00000482149.1:p.Val225Gly
NM_000162.3:c.677T>G	NP_000153.1:p.Val226Gly
NM_033507.1:c.680T>G	NP_277042.1:p.Val227Gly
NM_033508.1:c.674T>G	NP_277043.1:p.Val225Gly
XR_927223.1:n.277A>C
NM_000162.4:c.677T>G	NP_000153.1:p.Val226Gly
NM_001354800.1:c.677T>G	NP_001341729.1:p.Val226Gly
NM_033507.2:c.680T>G	NP_277042.1:p.Val227Gly
NM_033508.2:c.674T>G	NP_277043.1:p.Val225Gly
XR_927223.2:n.277A>C
NM_000162.5:c.677T>G MANE Select	NP_000153.1:p.Val226Gly
NM_033507.3:c.680T>G	NP_277042.1:p.Val227Gly
NM_033508.3:c.674T>G	NP_277043.1:p.Val225Gly