Canonical Allele Identifier: CA2455894172

Gene: GRIA3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.123428027T= , CM000685.2:g.123428027T=	GRCh38
NC_000023.10:g.122561878T= , CM000685.1:g.122561878T=	GRCh37
NC_000023.9:g.122389559T=	NCBI36
NG_009377.2:g.248785T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000620443.2:c.1964T= MANE Select	ENSP00000478489.1:p.Phe655=
ENST00000622768.5:c.1964T= MANE Plus Clinical	ENSP00000481554.1:p.Phe655=
ENST00000541091.5:c.1964T=	ENSP00000446440.2:p.Phe655=
ENST00000620443.1:c.1964T=	ENSP00000478489.1:p.Phe655=
ENST00000620581.4:c.1964T=	ENSP00000481875.1:p.Phe655=
ENST00000622768.4:c.1964T=	ENSP00000481554.1:p.Phe655=
NM_000828.4:c.1964T=	NP_000819.3:p.Phe655=
NM_007325.4:c.1964T=	NP_015564.4:p.Phe655=
XR_938574.1:n.5217+9223A=
NM_007325.5:c.1964T= MANE Select	NP_015564.5:p.Phe655=
NM_000828.5:c.1964T= MANE Plus Clinical	NP_000819.4:p.Phe655=