Canonical Allele Identifier: CA383013040

Gene: GRIK4

Linked Data

• MyVariant Identifiers: chr11:g.120827655G>A (hg19) ; chr11:g.120956946G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.120956946G>A , CM000673.2:g.120956946G>A	GRCh38
NC_000011.9:g.120827655G>A , CM000673.1:g.120827655G>A	GRCh37
NC_000011.8:g.120332865G>A	NCBI36
NG_042194.1:g.450201G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000527524.8:c.1867G>A MANE Select	ENSP00000435648.2:p.Gly623Ser
ENST00000638419.1:c.1867G>A	ENSP00000492086.1:p.Gly623Ser
ENST00000438375.2:c.1867G>A	ENSP00000404063.2:p.Gly623Ser
ENST00000527524.6:c.1867G>A	ENSP00000435648.1:p.Gly623Ser
ENST00000533291.5:n.2265G>A
NM_001282470.2:c.1867G>A	NP_001269399.1:p.Gly623Ser
NM_001282473.2:c.1867G>A	NP_001269402.1:p.Gly623Ser
NM_014619.4:c.1867G>A	NP_055434.2:p.Gly623Ser
NR_133004.1:n.82+1012C>T
XM_011542783.1:c.2083G>A	XP_011541085.1:p.Gly695Ser
XM_011542784.1:c.1705G>A	XP_011541086.1:p.Gly569Ser
XM_011542785.1:c.2083G>A	XP_011541087.1:p.Gly695Ser
XM_011542786.1:c.1141G>A	XP_011541088.1:p.Gly381Ser
XM_011542787.1:c.1105G>A	XP_011541089.1:p.Gly369Ser
XM_011542788.1:c.1105G>A	XP_011541090.1:p.Gly369Ser
XR_948104.1:n.104+1012C>T
XM_011542784.2:c.1705G>A	XP_011541086.1:p.Gly569Ser
XM_011542786.2:c.1141G>A	XP_011541088.1:p.Gly381Ser
XM_011542787.2:c.1105G>A	XP_011541089.1:p.Gly369Ser
XM_017017621.2:c.1701-3963G>A	XP_016873110.1:n.1701-3963G>A
XM_017017622.2:c.1663G>A	XP_016873111.1:p.Gly555Ser
NM_014619.5:c.1867G>A MANE Select	NP_055434.2:p.Gly623Ser
NM_001282470.3:c.1867G>A	NP_001269399.1:p.Gly623Ser
NM_001282473.3:c.1867G>A	NP_001269402.1:p.Gly623Ser