Canonical Allele Identifier: CA2455894214
Gene: GRIA3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.123428209A= , CM000685.2:g.123428209A= GRCh38
NC_000023.10:g.122562060A= , CM000685.1:g.122562060A= GRCh37
NC_000023.9:g.122389741A= NCBI36
NG_009377.2:g.248967A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000620443.2:c.2076+70A= MANE Select ENSP00000478489.1:n.2076+70A=
ENST00000622768.5:c.2076+70A= MANE Plus Clinical ENSP00000481554.1:n.2076+70A=
ENST00000541091.5:c.2076+70A= ENSP00000446440.2:n.2076+70A=
ENST00000620443.1:c.2076+70A= ENSP00000478489.1:n.2076+70A=
ENST00000620581.4:c.2076+70A= ENSP00000481875.1:n.2076+70A=
ENST00000622768.4:c.2076+70A= ENSP00000481554.1:n.2076+70A=
NM_000828.4:c.2076+70A= NP_000819.3:n.2076+70A=
NM_007325.4:c.2076+70A= NP_015564.4:n.2076+70A=
XR_938574.1:n.5217+9041T=
NM_007325.5:c.2076+70A= MANE Select NP_015564.5:n.2076+70A=
NM_000828.5:c.2076+70A= MANE Plus Clinical NP_000819.4:n.2076+70A=
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