Canonical Allele Identifier: CA414259862
Gene: GRIA3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.123428032A>C , CM000685.2:g.123428032A>C GRCh38
NC_000023.10:g.122561883A>C , CM000685.1:g.122561883A>C GRCh37
NC_000023.9:g.122389564A>C NCBI36
NG_009377.2:g.248790A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000620443.2:c.1969A>C MANE Select ENSP00000478489.1:p.Thr657Pro
ENST00000622768.5:c.1969A>C MANE Plus Clinical ENSP00000481554.1:p.Thr657Pro
ENST00000541091.5:c.1969A>C ENSP00000446440.2:p.Thr657Pro
ENST00000620443.1:c.1969A>C ENSP00000478489.1:p.Thr657Pro
ENST00000620581.4:c.1969A>C ENSP00000481875.1:p.Thr657Pro
ENST00000622768.4:c.1969A>C ENSP00000481554.1:p.Thr657Pro
NM_000828.4:c.1969A>C NP_000819.3:p.Thr657Pro
NM_007325.4:c.1969A>C NP_015564.4:p.Thr657Pro
XR_938574.1:n.5217+9218T>G
NM_007325.5:c.1969A>C MANE Select NP_015564.5:p.Thr657Pro
NM_000828.5:c.1969A>C MANE Plus Clinical NP_000819.4:p.Thr657Pro