Canonical Allele Identifier: CA2004583301

Gene: GRIK4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.120792562G= , CM000673.2:g.120792562G=	GRCh38
NC_000011.9:g.120663271G= , CM000673.1:g.120663271G=	GRCh37
NC_000011.8:g.120168481G=	NCBI36
NG_042194.1:g.285817G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000527524.8:c.83-10131G= MANE Select	ENSP00000435648.2:n.83-10131G=
ENST00000638419.1:c.83-10131G=	ENSP00000492086.1:n.83-10131G=
ENST00000438375.2:c.83-10131G=	ENSP00000404063.2:n.83-10131G=
ENST00000526536.1:n.283-10131G=
ENST00000527524.6:c.83-10131G=	ENSP00000435648.1:n.83-10131G=
ENST00000533291.5:n.481-10131G=
NM_001282470.2:c.83-10131G=	NP_001269399.1:n.83-10131G=
NM_001282473.2:c.83-10131G=	NP_001269402.1:n.83-10131G=
NM_014619.4:c.83-10131G=	NP_055434.2:n.83-10131G=
XM_011542783.1:c.83-10131G=	XP_011541085.1:n.83-10131G=
XM_011542784.1:c.83-10131G=	XP_011541086.1:n.83-10131G=
XM_011542785.1:c.83-10131G=	XP_011541087.1:n.83-10131G=
XM_011542784.2:c.83-10131G=	XP_011541086.1:n.83-10131G=
XM_017017621.2:c.83-10131G=	XP_016873110.1:n.83-10131G=
XM_017017622.2:c.83-10131G=	XP_016873111.1:n.83-10131G=
NM_014619.5:c.83-10131G= MANE Select	NP_055434.2:n.83-10131G=
NM_001282470.3:c.83-10131G=	NP_001269399.1:n.83-10131G=
NM_001282473.3:c.83-10131G=	NP_001269402.1:n.83-10131G=