Canonical Allele Identifier: CA6325872

Gene: GRIK4

Linked Data

• dbSNP Id: rs772829772
• ExAC: 11:120827651 C / T
• gnomAD v4: 11-120956942-C-T
• MyVariant Identifiers: chr11:g.120827651C>T (hg19) ; chr11:g.120956942C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.120956942C>T , CM000673.2:g.120956942C>T	GRCh38
NC_000011.9:g.120827651C>T , CM000673.1:g.120827651C>T	GRCh37
NC_000011.8:g.120332861C>T	NCBI36
NG_042194.1:g.450197C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000527524.8:c.1863C>T MANE Select	ENSP00000435648.2:p.Val621=
ENST00000638419.1:c.1863C>T	ENSP00000492086.1:p.Val621=
ENST00000438375.2:c.1863C>T	ENSP00000404063.2:p.Val621=
ENST00000527524.6:c.1863C>T	ENSP00000435648.1:p.Val621=
ENST00000533291.5:n.2261C>T
NM_001282470.2:c.1863C>T	NP_001269399.1:p.Val621=
NM_001282473.2:c.1863C>T	NP_001269402.1:p.Val621=
NM_014619.4:c.1863C>T	NP_055434.2:p.Val621=
NR_133004.1:n.82+1016G>A
XM_011542783.1:c.2079C>T	XP_011541085.1:p.Val693=
XM_011542784.1:c.1701C>T	XP_011541086.1:p.Val567=
XM_011542785.1:c.2079C>T	XP_011541087.1:p.Val693=
XM_011542786.1:c.1137C>T	XP_011541088.1:p.Val379=
XM_011542787.1:c.1101C>T	XP_011541089.1:p.Val367=
XM_011542788.1:c.1101C>T	XP_011541090.1:p.Val367=
XR_948104.1:n.104+1016G>A
XM_011542784.2:c.1701C>T	XP_011541086.1:p.Val567=
XM_011542786.2:c.1137C>T	XP_011541088.1:p.Val379=
XM_011542787.2:c.1101C>T	XP_011541089.1:p.Val367=
XM_017017621.2:c.1701-3967C>T	XP_016873110.1:n.1701-3967C>T
XM_017017622.2:c.1659C>T	XP_016873111.1:p.Val553=
NM_014619.5:c.1863C>T MANE Select	NP_055434.2:p.Val621=
NM_001282470.3:c.1863C>T	NP_001269399.1:p.Val621=
NM_001282473.3:c.1863C>T	NP_001269402.1:p.Val621=