Canonical Allele Identifier: CA367399935

Gene: GCK

Linked Data

• ClinVar Variation Id: 1807278
• ClinVar RCV Id: RCV002475235
• dbSNP Id: rs2128819989
• MyVariant Identifiers: chr7:g.44186135A>C (hg19) ; chr7:g.44146536A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44146536A>C , CM000669.2:g.44146536A>C	GRCh38
NC_000007.13:g.44186135A>C , CM000669.1:g.44186135A>C	GRCh37
NC_000007.12:g.44152660A>C	NCBI36
NG_008847.1:g.47888T>G
NG_008847.2:g.56635T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*944T>G	ENSP00000379142.4:n.*944T>G
ENST00000616242.5:c.*66T>G	ENSP00000482149.2:n.*66T>G
ENST00000683378.1:n.172T>G
ENST00000345378.7:c.949T>G	ENSP00000223366.2:p.Phe317Val
ENST00000403799.8:c.946T>G MANE Select	ENSP00000384247.3:p.Phe316Val
ENST00000671824.1:c.1009T>G	ENSP00000500264.1:p.Phe337Val
ENST00000673284.1:c.946T>G	ENSP00000499852.1:p.Phe316Val
ENST00000345378.6:c.949T>G	ENSP00000223366.2:p.Phe317Val
ENST00000395796.7:c.943T>G	ENSP00000379142.3:p.Phe315Val
ENST00000403799.7:c.946T>G	ENSP00000384247.3:p.Phe316Val
ENST00000437084.1:c.895T>G	ENSP00000402840.1:p.Phe299Val
ENST00000473353.1:n.244T>G
ENST00000616242.4:c.943T>G	ENSP00000482149.1:p.Phe315Val
NM_000162.3:c.946T>G	NP_000153.1:p.Phe316Val
NM_033507.1:c.949T>G	NP_277042.1:p.Phe317Val
NM_033508.1:c.943T>G	NP_277043.1:p.Phe315Val
NM_000162.4:c.946T>G	NP_000153.1:p.Phe316Val
NM_001354800.1:c.946T>G	NP_001341729.1:p.Phe316Val
NM_001354801.1:c.8+83T>G	NP_001341730.1:n.8+83T>G
NM_033507.2:c.949T>G	NP_277042.1:p.Phe317Val
NM_033508.2:c.943T>G	NP_277043.1:p.Phe315Val
NM_000162.5:c.946T>G MANE Select	NP_000153.1:p.Phe316Val
NM_033507.3:c.949T>G	NP_277042.1:p.Phe317Val
NM_033508.3:c.943T>G	NP_277043.1:p.Phe315Val