Canonical Allele Identifier: CA2455894098

Gene: GRIA3

Linked Data

• dbSNP Id: rs2045598058

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.123427775_123427777del , CM000685.2:g.123427775_123427777del	GRCh38
NC_000023.10:g.122561626_122561628del , CM000685.1:g.122561626_122561628del	GRCh37
NC_000023.9:g.122389307_122389309del	NCBI36
NG_009377.2:g.248533_248535del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000620443.2:c.1878-166_1878-164del MANE Select	ENSP00000478489.1:n.1878-166_1878-164del
ENST00000622768.5:c.1878-166_1878-164del MANE Plus Clinical	ENSP00000481554.1:n.1878-166_1878-164del
ENST00000541091.5:c.1878-166_1878-164del	ENSP00000446440.2:n.1878-166_1878-164del
ENST00000620443.1:c.1878-166_1878-164del	ENSP00000478489.1:n.1878-166_1878-164del
ENST00000620581.4:c.1878-166_1878-164del	ENSP00000481875.1:n.1878-166_1878-164del
ENST00000622768.4:c.1878-166_1878-164del	ENSP00000481554.1:n.1878-166_1878-164del
NM_000828.4:c.1878-166_1878-164del	NP_000819.3:n.1878-166_1878-164del
NM_007325.4:c.1878-166_1878-164del	NP_015564.4:n.1878-166_1878-164del
XR_938574.1:n.5217+9478_5217+9480del
NM_007325.5:c.1878-166_1878-164del MANE Select	NP_015564.5:n.1878-166_1878-164del
NM_000828.5:c.1878-166_1878-164del MANE Plus Clinical	NP_000819.4:n.1878-166_1878-164del