Canonical Allele Identifier: CA2455905820

Gene: GRIA3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.123464915G= , CM000685.2:g.123464915G=	GRCh38
NC_000023.10:g.122598766G= , CM000685.1:g.122598766G=	GRCh37
NC_000023.9:g.122426447G=	NCBI36
NG_009377.2:g.285673G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000620443.2:c.2127G= MANE Select	ENSP00000478489.1:p.Ala709=
ENST00000622768.5:c.2127G= MANE Plus Clinical	ENSP00000481554.1:p.Ala709=
ENST00000541091.5:c.2127G=	ENSP00000446440.2:p.Ala709=
ENST00000620443.1:c.2127G=	ENSP00000478489.1:p.Ala709=
ENST00000620581.4:c.2127G=	ENSP00000481875.1:p.Ala709=
ENST00000622768.4:c.2127G=	ENSP00000481554.1:p.Ala709=
NM_000828.4:c.2127G=	NP_000819.3:p.Ala709=
NM_007325.4:c.2127G=	NP_015564.4:p.Ala709=
XR_938574.1:n.4959+1839C=
NM_007325.5:c.2127G= MANE Select	NP_015564.5:p.Ala709=
NM_000828.5:c.2127G= MANE Plus Clinical	NP_000819.4:p.Ala709=