Canonical Allele Identifier: CA15051095

Gene: GRIA3

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.123239256C>T , CM000685.2:g.123239256C>T	GRCh38
NC_000023.10:g.122373107C>T , CM000685.1:g.122373107C>T	GRCh37
NC_000023.9:g.122200788C>T	NCBI36
NG_009377.2:g.60014C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000620443.2:c.269-14047C>T MANE Select	ENSP00000478489.1:n.269-14047C>T
ENST00000622768.5:c.269-14047C>T MANE Plus Clinical	ENSP00000481554.1:n.269-14047C>T
ENST00000479118.1:n.245-14047C>T
ENST00000541091.5:c.269-14047C>T	ENSP00000446440.2:n.269-14047C>T
ENST00000620443.1:c.269-14047C>T	ENSP00000478489.1:n.269-14047C>T
ENST00000620581.4:c.269-14047C>T	ENSP00000481875.1:n.269-14047C>T
ENST00000622768.4:c.269-14047C>T	ENSP00000481554.1:n.269-14047C>T
NM_000828.4:c.269-14047C>T	NP_000819.3:n.269-14047C>T
NM_007325.4:c.269-14047C>T	NP_015564.4:n.269-14047C>T
NM_007325.5:c.269-14047C>T MANE Select	NP_015564.5:n.269-14047C>T
NM_000828.5:c.269-14047C>T MANE Plus Clinical	NP_000819.4:n.269-14047C>T