Canonical Allele Identifier: CA2004662654

Gene: GRIK4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.120966045G= , CM000673.2:g.120966045G=	GRCh38
NC_000011.9:g.120836754G= , CM000673.1:g.120836754G=	GRCh37
NC_000011.8:g.120341964G=	NCBI36
NG_042194.1:g.459300G=

Transcript Alleles

HGVS	Amino-acid Change
NM_014619.5:c.2267-1150G= MANE Select	NP_055434.2:n.2267-1150G=
ENST00000527524.8:c.2267-1150G= MANE Select	ENSP00000435648.2:n.2267-1150G=
NM_001282470.2:c.2267-1150G=	NP_001269399.1:n.2267-1150G=
NM_001282470.3:c.2267-1150G=	NP_001269399.1:n.2267-1150G=
NM_014619.4:c.2267-1150G=	NP_055434.2:n.2267-1150G=
ENST00000438375.2:c.2267-1150G=	ENSP00000404063.2:n.2267-1150G=
ENST00000527524.6:c.2267-1150G=	ENSP00000435648.1:n.2267-1150G=
ENST00000638419.1:c.2267-1150G=	ENSP00000492086.1:n.2267-1150G=
XM_011542783.1:c.2483-1150G=	XP_011541085.1:n.2483-1150G=
XM_011542784.1:c.2105-1150G=	XP_011541086.1:n.2105-1150G=
XM_011542784.2:c.2105-1150G=	XP_011541086.1:n.2105-1150G=
XM_011542785.1:c.2483-1150G=	XP_011541087.1:n.2483-1150G=
XM_011542786.1:c.1541-1150G=	XP_011541088.1:n.1541-1150G=
XM_011542786.2:c.1541-1150G=	XP_011541088.1:n.1541-1150G=
XM_011542787.1:c.1505-1150G=	XP_011541089.1:n.1505-1150G=
XM_011542787.2:c.1505-1150G=	XP_011541089.1:n.1505-1150G=
XM_011542788.1:c.1505-1150G=	XP_011541090.1:n.1505-1150G=
XM_017017621.2:c.2093-1150G=	XP_016873110.1:n.2093-1150G=
XM_017017622.2:c.2063-1150G=	XP_016873111.1:n.2063-1150G=