Canonical Allele Identifier: CA13399769

Gene: GRIK4

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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