Canonical Allele Identifier: CA2004656309

Gene: GRIK4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.120956944G= , CM000673.2:g.120956944G=	GRCh38
NC_000011.9:g.120827653G= , CM000673.1:g.120827653G=	GRCh37
NC_000011.8:g.120332863G=	NCBI36
NG_042194.1:g.450199G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000527524.8:c.1865G= MANE Select	ENSP00000435648.2:p.Ser622=
ENST00000638419.1:c.1865G=	ENSP00000492086.1:p.Ser622=
ENST00000438375.2:c.1865G=	ENSP00000404063.2:p.Ser622=
ENST00000527524.6:c.1865G=	ENSP00000435648.1:p.Ser622=
ENST00000533291.5:n.2263G=
NM_001282470.2:c.1865G=	NP_001269399.1:p.Ser622=
NM_001282473.2:c.1865G=	NP_001269402.1:p.Ser622=
NM_014619.4:c.1865G=	NP_055434.2:p.Ser622=
NR_133004.1:n.82+1014C=
XM_011542783.1:c.2081G=	XP_011541085.1:p.Ser694=
XM_011542784.1:c.1703G=	XP_011541086.1:p.Ser568=
XM_011542785.1:c.2081G=	XP_011541087.1:p.Ser694=
XM_011542786.1:c.1139G=	XP_011541088.1:p.Ser380=
XM_011542787.1:c.1103G=	XP_011541089.1:p.Ser368=
XM_011542788.1:c.1103G=	XP_011541090.1:p.Ser368=
XR_948104.1:n.104+1014C=
XM_011542784.2:c.1703G=	XP_011541086.1:p.Ser568=
XM_011542786.2:c.1139G=	XP_011541088.1:p.Ser380=
XM_011542787.2:c.1103G=	XP_011541089.1:p.Ser368=
XM_017017621.2:c.1701-3965G=	XP_016873110.1:n.1701-3965G=
XM_017017622.2:c.1661G=	XP_016873111.1:p.Ser554=
NM_014619.5:c.1865G= MANE Select	NP_055434.2:p.Ser622=
NM_001282470.3:c.1865G=	NP_001269399.1:p.Ser622=
NM_001282473.3:c.1865G=	NP_001269402.1:p.Ser622=