Canonical Allele Identifier: CA383013044

Gene: GRIK4

Linked Data

• gnomAD v4: 11-120956947-G-T
• MyVariant Identifiers: chr11:g.120827656G>T (hg19) ; chr11:g.120956947G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.120956947G>T , CM000673.2:g.120956947G>T	GRCh38
NC_000011.9:g.120827656G>T , CM000673.1:g.120827656G>T	GRCh37
NC_000011.8:g.120332866G>T	NCBI36
NG_042194.1:g.450202G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000527524.8:c.1868G>T MANE Select	ENSP00000435648.2:p.Gly623Val
ENST00000638419.1:c.1868G>T	ENSP00000492086.1:p.Gly623Val
ENST00000438375.2:c.1868G>T	ENSP00000404063.2:p.Gly623Val
ENST00000527524.6:c.1868G>T	ENSP00000435648.1:p.Gly623Val
ENST00000533291.5:n.2266G>T
NM_001282470.2:c.1868G>T	NP_001269399.1:p.Gly623Val
NM_001282473.2:c.1868G>T	NP_001269402.1:p.Gly623Val
NM_014619.4:c.1868G>T	NP_055434.2:p.Gly623Val
NR_133004.1:n.82+1011C>A
XM_011542783.1:c.2084G>T	XP_011541085.1:p.Gly695Val
XM_011542784.1:c.1706G>T	XP_011541086.1:p.Gly569Val
XM_011542785.1:c.2084G>T	XP_011541087.1:p.Gly695Val
XM_011542786.1:c.1142G>T	XP_011541088.1:p.Gly381Val
XM_011542787.1:c.1106G>T	XP_011541089.1:p.Gly369Val
XM_011542788.1:c.1106G>T	XP_011541090.1:p.Gly369Val
XR_948104.1:n.104+1011C>A
XM_011542784.2:c.1706G>T	XP_011541086.1:p.Gly569Val
XM_011542786.2:c.1142G>T	XP_011541088.1:p.Gly381Val
XM_011542787.2:c.1106G>T	XP_011541089.1:p.Gly369Val
XM_017017621.2:c.1701-3962G>T	XP_016873110.1:n.1701-3962G>T
XM_017017622.2:c.1664G>T	XP_016873111.1:p.Gly555Val
NM_014619.5:c.1868G>T MANE Select	NP_055434.2:p.Gly623Val
NM_001282470.3:c.1868G>T	NP_001269399.1:p.Gly623Val
NM_001282473.3:c.1868G>T	NP_001269402.1:p.Gly623Val