Canonical Allele Identifier: CA367399907

Gene: GCK

Linked Data

• MyVariant Identifiers: chr7:g.44186128C>A (hg19) ; chr7:g.44146529C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44146529C>A , CM000669.2:g.44146529C>A	GRCh38
NC_000007.13:g.44186128C>A , CM000669.1:g.44186128C>A	GRCh37
NC_000007.12:g.44152653C>A	NCBI36
NG_008847.1:g.47895G>T
NG_008847.2:g.56642G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*951G>T	ENSP00000379142.4:n.*951G>T
ENST00000616242.5:c.*73G>T	ENSP00000482149.2:n.*73G>T
ENST00000683378.1:n.179G>T
ENST00000345378.7:c.956G>T	ENSP00000223366.2:p.Gly319Val
ENST00000403799.8:c.953G>T MANE Select	ENSP00000384247.3:p.Gly318Val
ENST00000671824.1:c.1016G>T	ENSP00000500264.1:p.Gly339Val
ENST00000673284.1:c.953G>T	ENSP00000499852.1:p.Gly318Val
ENST00000345378.6:c.956G>T	ENSP00000223366.2:p.Gly319Val
ENST00000395796.7:c.950G>T	ENSP00000379142.3:p.Gly317Val
ENST00000403799.7:c.953G>T	ENSP00000384247.3:p.Gly318Val
ENST00000437084.1:c.902G>T	ENSP00000402840.1:p.Gly301Val
ENST00000473353.1:n.251G>T
ENST00000616242.4:c.950G>T	ENSP00000482149.1:p.Gly317Val
NM_000162.3:c.953G>T	NP_000153.1:p.Gly318Val
NM_033507.1:c.956G>T	NP_277042.1:p.Gly319Val
NM_033508.1:c.950G>T	NP_277043.1:p.Gly317Val
NM_000162.4:c.953G>T	NP_000153.1:p.Gly318Val
NM_001354800.1:c.953G>T	NP_001341729.1:p.Gly318Val
NM_001354801.1:c.8+90G>T	NP_001341730.1:n.8+90G>T
NM_033507.2:c.956G>T	NP_277042.1:p.Gly319Val
NM_033508.2:c.950G>T	NP_277043.1:p.Gly317Val
NM_000162.5:c.953G>T MANE Select	NP_000153.1:p.Gly318Val
NM_033507.3:c.956G>T	NP_277042.1:p.Gly319Val
NM_033508.3:c.950G>T	NP_277043.1:p.Gly317Val