Canonical Allele Identifier: CA15311265

Gene: GRIA2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.157364445T>C , CM000666.2:g.157364445T>C	GRCh38
NC_000004.11:g.158285597T>C , CM000666.1:g.158285597T>C	GRCh37
NC_000004.10:g.158505047T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703717.1:c.*1014T>C	ENSP00000515446.1:n.*1014T>C
ENST00000703718.1:c.*1014T>C	ENSP00000515447.1:n.*1014T>C
ENST00000703719.1:c.3233T>C
ENST00000703751.1:c.*1225T>C	ENSP00000515460.1:n.*1225T>C
ENST00000703754.1:c.*120+894T>C	ENSP00000515463.1:n.*120+894T>C
ENST00000703761.1:c.*846T>C	ENSP00000515469.1:n.*846T>C
ENST00000703765.1:c.*1014T>C	ENSP00000515472.1:n.*1014T>C
ENST00000703768.1:c.2534T>C
ENST00000264426.14:c.*1014T>C MANE Select	ENSP00000264426.9:n.*1014T>C
ENST00000296526.12:c.*1014T>C	ENSP00000296526.7:n.*1014T>C
ENST00000296526.11:c.*1014T>C	ENSP00000296526.7:n.*1014T>C
ENST00000393815.6:c.*1014T>C	ENSP00000377403.2:n.*1014T>C
NM_000826.3:c.*1014T>C	NP_000817.2:n.*1014T>C
NM_001083619.1:c.*1014T>C	NP_001077088.1:n.*1014T>C
NM_001083620.1:c.*1014T>C	NP_001077089.1:n.*1014T>C
XR_001741212.2:n.4201T>C
XR_002959808.1:n.9485A>G
NM_000826.4:c.*1014T>C	NP_000817.3:n.*1014T>C
NM_000826.6:c.*1014T>C	NP_000817.5:n.*1014T>C
NM_001083619.3:c.*1014T>C MANE Select	NP_001077088.2:n.*1014T>C
NM_001083620.3:c.*1014T>C	NP_001077089.2:n.*1014T>C
NM_001379000.3:c.*1014T>C	NP_001365929.3:n.*1014T>C
NM_001379001.3:c.*1014T>C	NP_001365930.3:n.*1014T>C