Canonical Allele Identifier: CA229739836

Gene: GRIK4

Linked Data

• dbSNP Id: rs4245040
• gnomAD v3: 11-120649920-T-A
• gnomAD v4: 11-120649920-T-A
• MyVariant Identifiers: chr11:g.120520629T>A (hg19) ; chr11:g.120649920T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.120649920T>A , CM000673.2:g.120649920T>A	GRCh38
NC_000011.9:g.120520629T>A , CM000673.1:g.120520629T>A	GRCh37
NC_000011.8:g.120025839T>A	NCBI36
NG_042194.1:g.143175T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000527524.8:c.-158-3765T>A MANE Select	ENSP00000435648.2:n.-158-3765T>A
ENST00000638419.1:c.-155-3768T>A	ENSP00000492086.1:n.-155-3768T>A
ENST00000438375.2:c.-50-10349T>A	ENSP00000404063.2:n.-50-10349T>A
ENST00000526536.1:n.282+73357T>A
ENST00000527524.6:c.-158-3765T>A	ENSP00000435648.1:n.-158-3765T>A
ENST00000533291.5:n.241-3765T>A
NM_001282470.2:c.-50-10349T>A	NP_001269399.1:n.-50-10349T>A
NM_001282473.2:c.-158-3765T>A	NP_001269402.1:n.-158-3765T>A
NM_014619.4:c.-158-3765T>A	NP_055434.2:n.-158-3765T>A
NM_014619.5:c.-158-3765T>A MANE Select	NP_055434.2:n.-158-3765T>A
NM_001282470.3:c.-50-10349T>A	NP_001269399.1:n.-50-10349T>A
NM_001282473.3:c.-158-3765T>A	NP_001269402.1:n.-158-3765T>A