Canonical Allele Identifier: CA2455840596

Gene: GRIA3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.123253500T= , CM000685.2:g.123253500T=	GRCh38
NC_000023.10:g.122387351T= , CM000685.1:g.122387351T=	GRCh37
NC_000023.9:g.122215032T=	NCBI36
NG_009377.2:g.74258T=

Transcript Alleles

HGVS	Amino-acid Change
NM_007325.5:c.466T= MANE Select	NP_015564.5:p.Tyr156=
ENST00000620443.2:c.466T= MANE Select	ENSP00000478489.1:p.Tyr156=
NM_000828.5:c.466T= MANE Plus Clinical	NP_000819.4:p.Tyr156=
ENST00000622768.5:c.466T= MANE Plus Clinical	ENSP00000481554.1:p.Tyr156=
NM_000828.4:c.466T=	NP_000819.3:p.Tyr156=
NM_007325.4:c.466T=	NP_015564.4:p.Tyr156=
ENST00000479118.1:n.442T=
ENST00000541091.5:c.466T=	ENSP00000446440.2:p.Tyr156=
ENST00000620443.1:c.466T=	ENSP00000478489.1:p.Tyr156=
ENST00000620581.4:c.466T=	ENSP00000481875.1:p.Tyr156=
ENST00000622768.4:c.466T=	ENSP00000481554.1:p.Tyr156=