Canonical Allele Identifier: CA10575670

Gene: GRIA3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.123184534G= , CM000685.2:g.123184534G=	GRCh38
NG_009377.2:g.5292G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000620443.2:c.-2G= MANE Select	ENSP00000478489.1:n.-2G=
ENST00000622768.5:c.-2G= MANE Plus Clinical	ENSP00000481554.1:n.-2G=
ENST00000541091.5:c.-2G=	ENSP00000446440.2:n.-2G=
ENST00000611689.4:c.-2G=	ENSP00000478758.1:n.-2G=
ENST00000616590.4:c.-2G=	ENSP00000479607.1:n.-2G=
ENST00000620443.1:c.-2G=	ENSP00000478489.1:n.-2G=
ENST00000620581.4:c.-2G=	ENSP00000481875.1:n.-2G=
ENST00000622768.4:c.-2G=	ENSP00000481554.1:n.-2G=
NM_000828.4:c.-2G=	NP_000819.3:n.-2G=
NM_001256743.1:c.-2G=	NP_001243672.1:n.-2G=
NM_007325.4:c.-2G=	NP_015564.4:n.-2G=
NM_001256743.2:c.-2G=	NP_001243672.1:n.-2G=
NM_007325.5:c.-2G= MANE Select	NP_015564.5:n.-2G=
NM_000828.5:c.-2G= MANE Plus Clinical	NP_000819.4:n.-2G=