Canonical Allele Identifier: CA13552699

Gene: GRIK4

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.120938751T>G , CM000673.2:g.120938751T>G	GRCh38
NC_000011.9:g.120809460T>G , CM000673.1:g.120809460T>G	GRCh37
NC_000011.8:g.120314670T>G	NCBI36
NG_042194.1:g.432006T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527524.8:c.1477-1596T>G MANE Select	ENSP00000435648.2:n.1477-1596T>G
ENST00000638419.1:c.1477-1596T>G	ENSP00000492086.1:n.1477-1596T>G
ENST00000438375.2:c.1477-1596T>G	ENSP00000404063.2:n.1477-1596T>G
ENST00000527524.6:c.1477-1596T>G	ENSP00000435648.1:n.1477-1596T>G
ENST00000533291.5:n.1875-1596T>G
NM_001282470.2:c.1477-1596T>G	NP_001269399.1:n.1477-1596T>G
NM_001282473.2:c.1477-1596T>G	NP_001269402.1:n.1477-1596T>G
NM_014619.4:c.1477-1596T>G	NP_055434.2:n.1477-1596T>G
XM_011542783.1:c.1693-1596T>G	XP_011541085.1:n.1693-1596T>G
XM_011542784.1:c.1315-1596T>G	XP_011541086.1:n.1315-1596T>G
XM_011542785.1:c.1693-1596T>G	XP_011541087.1:n.1693-1596T>G
XM_011542786.1:c.751-1596T>G	XP_011541088.1:n.751-1596T>G
XM_011542787.1:c.715-1596T>G	XP_011541089.1:n.715-1596T>G
XM_011542788.1:c.715-1596T>G	XP_011541090.1:n.715-1596T>G
XM_011542784.2:c.1315-1596T>G	XP_011541086.1:n.1315-1596T>G
XM_011542786.2:c.751-1596T>G	XP_011541088.1:n.751-1596T>G
XM_011542787.2:c.715-1596T>G	XP_011541089.1:n.715-1596T>G
XM_017017621.2:c.1477-1596T>G	XP_016873110.1:n.1477-1596T>G
XM_017017622.2:c.1273-1596T>G	XP_016873111.1:n.1273-1596T>G
NM_014619.5:c.1477-1596T>G MANE Select	NP_055434.2:n.1477-1596T>G
NM_001282470.3:c.1477-1596T>G	NP_001269399.1:n.1477-1596T>G
NM_001282473.3:c.1477-1596T>G	NP_001269402.1:n.1477-1596T>G