Canonical Allele Identifier: CA2004583313
Gene: GRIK4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.120792579T= , CM000673.2:g.120792579T= GRCh38
NC_000011.9:g.120663288T= , CM000673.1:g.120663288T= GRCh37
NC_000011.8:g.120168498T= NCBI36
NG_042194.1:g.285834T=

Transcript Alleles

HGVS Amino-acid change
ENST00000527524.8:c.83-10114T= MANE Select ENSP00000435648.2:n.83-10114T=
ENST00000638419.1:c.83-10114T= ENSP00000492086.1:n.83-10114T=
ENST00000438375.2:c.83-10114T= ENSP00000404063.2:n.83-10114T=
ENST00000526536.1:n.283-10114T=
ENST00000527524.6:c.83-10114T= ENSP00000435648.1:n.83-10114T=
ENST00000533291.5:n.481-10114T=
NM_001282470.2:c.83-10114T= NP_001269399.1:n.83-10114T=
NM_001282473.2:c.83-10114T= NP_001269402.1:n.83-10114T=
NM_014619.4:c.83-10114T= NP_055434.2:n.83-10114T=
XM_011542783.1:c.83-10114T= XP_011541085.1:n.83-10114T=
XM_011542784.1:c.83-10114T= XP_011541086.1:n.83-10114T=
XM_011542785.1:c.83-10114T= XP_011541087.1:n.83-10114T=
XM_011542784.2:c.83-10114T= XP_011541086.1:n.83-10114T=
XM_017017621.2:c.83-10114T= XP_016873110.1:n.83-10114T=
XM_017017622.2:c.83-10114T= XP_016873111.1:n.83-10114T=
NM_014619.5:c.83-10114T= MANE Select NP_055434.2:n.83-10114T=
NM_001282470.3:c.83-10114T= NP_001269399.1:n.83-10114T=
NM_001282473.3:c.83-10114T= NP_001269402.1:n.83-10114T=