Canonical Allele Identifier: CA367399885

Gene: GCK

Linked Data

• MyVariant Identifiers: chr7:g.44186122G>T (hg19) ; chr7:g.44146523G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44146523G>T , CM000669.2:g.44146523G>T	GRCh38
NC_000007.13:g.44186122G>T , CM000669.1:g.44186122G>T	GRCh37
NC_000007.12:g.44152647G>T	NCBI36
NG_008847.1:g.47901C>A
NG_008847.2:g.56648C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*957C>A	ENSP00000379142.4:n.*957C>A
ENST00000616242.5:c.*79C>A	ENSP00000482149.2:n.*79C>A
ENST00000683378.1:n.185C>A
ENST00000345378.7:c.962C>A	ENSP00000223366.2:p.Ala321Asp
ENST00000403799.8:c.959C>A MANE Select	ENSP00000384247.3:p.Ala320Asp
ENST00000671824.1:c.1022C>A	ENSP00000500264.1:p.Ala341Asp
ENST00000673284.1:c.959C>A	ENSP00000499852.1:p.Ala320Asp
ENST00000345378.6:c.962C>A	ENSP00000223366.2:p.Ala321Asp
ENST00000395796.7:c.956C>A	ENSP00000379142.3:p.Ala319Asp
ENST00000403799.7:c.959C>A	ENSP00000384247.3:p.Ala320Asp
ENST00000437084.1:c.908C>A	ENSP00000402840.1:p.Ala303Asp
ENST00000473353.1:n.257C>A
ENST00000616242.4:c.956C>A	ENSP00000482149.1:p.Ala319Asp
NM_000162.3:c.959C>A	NP_000153.1:p.Ala320Asp
NM_033507.1:c.962C>A	NP_277042.1:p.Ala321Asp
NM_033508.1:c.956C>A	NP_277043.1:p.Ala319Asp
NM_000162.4:c.959C>A	NP_000153.1:p.Ala320Asp
NM_001354800.1:c.959C>A	NP_001341729.1:p.Ala320Asp
NM_001354801.1:c.8+96C>A	NP_001341730.1:n.8+96C>A
NM_033507.2:c.962C>A	NP_277042.1:p.Ala321Asp
NM_033508.2:c.956C>A	NP_277043.1:p.Ala319Asp
NM_000162.5:c.959C>A MANE Select	NP_000153.1:p.Ala320Asp
NM_033507.3:c.962C>A	NP_277042.1:p.Ala321Asp
NM_033508.3:c.956C>A	NP_277043.1:p.Ala319Asp