Canonical Allele Identifier: CA2455905801

Gene: GRIA3

Linked Data

• dbSNP Id: rs2045826336

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.123464835_123464843del , CM000685.2:g.123464835_123464843del	GRCh38
NC_000023.10:g.122598686_122598694del , CM000685.1:g.122598686_122598694del	GRCh37
NC_000023.9:g.122426367_122426375del	NCBI36
NG_009377.2:g.285593_285601del

Transcript Alleles

HGVS	Amino-acid change
ENST00000620443.2:c.2077-30_2077-22del MANE Select	ENSP00000478489.1:n.2077-30_2077-22del
ENST00000622768.5:c.2077-30_2077-22del MANE Plus Clinical	ENSP00000481554.1:n.2077-30_2077-22del
ENST00000541091.5:c.2077-30_2077-22del	ENSP00000446440.2:n.2077-30_2077-22del
ENST00000620443.1:c.2077-30_2077-22del	ENSP00000478489.1:n.2077-30_2077-22del
ENST00000620581.4:c.2077-30_2077-22del	ENSP00000481875.1:n.2077-30_2077-22del
ENST00000622768.4:c.2077-30_2077-22del	ENSP00000481554.1:n.2077-30_2077-22del
NM_000828.4:c.2077-30_2077-22del	NP_000819.3:n.2077-30_2077-22del
NM_007325.4:c.2077-30_2077-22del	NP_015564.4:n.2077-30_2077-22del
XR_938574.1:n.4959+1912_4959+1920del
NM_007325.5:c.2077-30_2077-22del MANE Select	NP_015564.5:n.2077-30_2077-22del
NM_000828.5:c.2077-30_2077-22del MANE Plus Clinical	NP_000819.4:n.2077-30_2077-22del