Canonical Allele Identifier: CA2455857816

Gene: GRIA3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.123307669C= , CM000685.2:g.123307669C=	GRCh38
NC_000023.10:g.122441520C= , CM000685.1:g.122441520C=	GRCh37
NC_000023.9:g.122269201C=	NCBI36
NG_009377.2:g.128427C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000620443.2:c.509-18357C= MANE Select	ENSP00000478489.1:n.509-18357C=
ENST00000622768.5:c.509-18357C= MANE Plus Clinical	ENSP00000481554.1:n.509-18357C=
ENST00000541091.5:c.509-18357C=	ENSP00000446440.2:n.509-18357C=
ENST00000620443.1:c.509-18357C=	ENSP00000478489.1:n.509-18357C=
ENST00000620581.4:c.509-18357C=	ENSP00000481875.1:n.509-18357C=
ENST00000622768.4:c.509-18357C=	ENSP00000481554.1:n.509-18357C=
NM_000828.4:c.509-18357C=	NP_000819.3:n.509-18357C=
NM_007325.4:c.509-18357C=	NP_015564.4:n.509-18357C=
NM_007325.5:c.509-18357C= MANE Select	NP_015564.5:n.509-18357C=
NM_000828.5:c.509-18357C= MANE Plus Clinical	NP_000819.4:n.509-18357C=