Canonical Allele Identifier: CA2004515560
Gene: GRIK4 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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