Canonical Allele Identifier: CA2455910639

Gene: GRIA3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.123482856G= , CM000685.2:g.123482856G=	GRCh38
NC_000023.10:g.122616707G= , CM000685.1:g.122616707G=	GRCh37
NC_000023.9:g.122444388G=	NCBI36
NG_009377.2:g.303614G=

Transcript Alleles

HGVS	Amino-acid Change
NM_007325.5:c.2497G= MANE Select	NP_015564.5:p.Gly833=
ENST00000620443.2:c.2497G= MANE Select	ENSP00000478489.1:p.Gly833=
NM_000828.5:c.2497G= MANE Plus Clinical	NP_000819.4:p.Gly833=
ENST00000622768.5:c.2497G= MANE Plus Clinical	ENSP00000481554.1:p.Gly833=
NM_000828.4:c.2497G=	NP_000819.3:p.Gly833=
NM_007325.4:c.2497G=	NP_015564.4:p.Gly833=
ENST00000460123.1:n.134G=
ENST00000541091.5:c.2497G=	ENSP00000446440.2:p.Gly833=
ENST00000620443.1:c.2497G=	ENSP00000478489.1:p.Gly833=
ENST00000620581.4:c.*137G=	ENSP00000481875.1:n.*137G=
ENST00000622768.4:c.2497G=	ENSP00000481554.1:p.Gly833=