Canonical Allele Identifier: CA2455894171
Gene: GRIA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.123428020G= , CM000685.2:g.123428020G= GRCh38
NC_000023.10:g.122561871G= , CM000685.1:g.122561871G= GRCh37
NC_000023.9:g.122389552G= NCBI36
NG_009377.2:g.248778G=

Transcript Alleles

HGVS Amino-acid change
ENST00000620443.2:c.1957G= MANE Select ENSP00000478489.1:p.Ala653=
ENST00000622768.5:c.1957G= MANE Plus Clinical ENSP00000481554.1:p.Ala653=
ENST00000541091.5:c.1957G= ENSP00000446440.2:p.Ala653=
ENST00000620443.1:c.1957G= ENSP00000478489.1:p.Ala653=
ENST00000620581.4:c.1957G= ENSP00000481875.1:p.Ala653=
ENST00000622768.4:c.1957G= ENSP00000481554.1:p.Ala653=
NM_000828.4:c.1957G= NP_000819.3:p.Ala653=
NM_007325.4:c.1957G= NP_015564.4:p.Ala653=
XR_938574.1:n.5217+9230C=
NM_007325.5:c.1957G= MANE Select NP_015564.5:p.Ala653=
NM_000828.5:c.1957G= MANE Plus Clinical NP_000819.4:p.Ala653=