Canonical Allele Identifier: CA394715044

Gene: GRIN2A

Linked Data

• dbSNP Id: rs2142387278
• MyVariant Identifiers: chr16:g.10273859T>G (hg19) ; chr16:g.10180002T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10180002T>G , CM000678.2:g.10180002T>G	GRCh38
NC_000016.9:g.10273859T>G , CM000678.1:g.10273859T>G	GRCh37
NC_000016.8:g.10181360T>G	NCBI36
NG_011812.1:g.7753A>C
NG_011812.2:g.7753A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.410A>C MANE Select	ENSP00000332549.3:p.Asp137Ala
ENST00000637334.1:n.89A>C
ENST00000637393.1:c.2A>C	ENSP00000490232.1:p.Asp1Ala
ENST00000675189.1:n.894A>C
ENST00000675398.1:c.410A>C	ENSP00000502752.1:p.Asp137Ala
ENST00000676032.1:n.843A>C
ENST00000330684.3:c.410A>C	ENSP00000332549.3:p.Asp137Ala
ENST00000396573.6:c.410A>C	ENSP00000379818.2:p.Asp137Ala
ENST00000562109.5:c.410A>C	ENSP00000454998.1:p.Asp137Ala
ENST00000566665.1:n.811A>C
NM_000833.4:c.410A>C	NP_000824.1:p.Asp137Ala
NM_001134407.2:c.410A>C	NP_001127879.1:p.Asp137Ala
NM_001134408.2:c.410A>C	NP_001127880.1:p.Asp137Ala
XM_011522461.1:c.410A>C	XP_011520763.1:p.Asp137Ala
XM_011522461.3:c.410A>C	XP_011520763.1:p.Asp137Ala
XM_017023172.1:c.566A>C	XP_016878661.1:p.Asp189Ala
XM_017023173.1:c.566A>C	XP_016878662.1:p.Asp189Ala
NM_001134407.3:c.410A>C MANE Select	NP_001127879.1:p.Asp137Ala
NM_000833.5:c.410A>C	NP_000824.1:p.Asp137Ala