Canonical Allele Identifier: CA394799055

Gene: GRIN2A

Linked Data

• MyVariant Identifiers: chr16:g.10032276A>C (hg19) ; chr16:g.9938419A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9938419A>C , CM000678.2:g.9938419A>C	GRCh38
NC_000016.9:g.10032276A>C , CM000678.1:g.10032276A>C	GRCh37
NC_000016.8:g.9939777A>C	NCBI36
NG_011812.1:g.249336T>G
NG_011812.2:g.249336T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000330684.4:c.547T>G MANE Select	ENSP00000332549.3:p.Phe183Val
ENST00000535259.6:c.76T>G	ENSP00000441572.3:p.Phe26Val
ENST00000636273.2:n.140T>G
ENST00000637393.1:c.139T>G	ENSP00000490232.1:p.Phe47Val
ENST00000674742.1:c.76T>G	ENSP00000502200.1:p.Phe26Val
ENST00000675189.1:n.1031T>G
ENST00000675398.1:c.547T>G	ENSP00000502752.1:p.Phe183Val
ENST00000330684.3:c.547T>G	ENSP00000332549.3:p.Phe183Val
ENST00000396573.6:c.547T>G	ENSP00000379818.2:p.Phe183Val
ENST00000396575.6:c.136T>G	ENSP00000379820.3:p.Phe46Val
ENST00000461292.3:n.186T>G
ENST00000535259.5:c.136T>G	ENSP00000441572.2:p.Phe46Val
ENST00000562109.5:c.547T>G	ENSP00000454998.1:p.Phe183Val
ENST00000566670.2:n.389T>G
ENST00000566683.1:n.241-47319T>G
ENST00000568247.3:n.439T>G
NM_000833.4:c.547T>G	NP_000824.1:p.Phe183Val
NM_001134407.2:c.547T>G	NP_001127879.1:p.Phe183Val
NM_001134408.2:c.547T>G	NP_001127880.1:p.Phe183Val
XM_011522456.1:c.388T>G	XP_011520758.1:p.Phe130Val
XM_011522457.1:c.289T>G	XP_011520759.1:p.Phe97Val
XM_011522458.1:c.76T>G	XP_011520760.1:p.Phe26Val
XM_011522459.1:c.76T>G	XP_011520761.1:p.Phe26Val
XM_011522460.1:c.76T>G	XP_011520762.1:p.Phe26Val
XM_011522461.1:c.547T>G	XP_011520763.1:p.Phe183Val
XM_011522458.3:c.76T>G	XP_011520760.1:p.Phe26Val
XM_011522461.3:c.547T>G	XP_011520763.1:p.Phe183Val
XM_017023172.1:c.703T>G	XP_016878661.1:p.Phe235Val
XM_017023173.1:c.703T>G	XP_016878662.1:p.Phe235Val
NM_001134407.3:c.547T>G MANE Select	NP_001127879.1:p.Phe183Val
NM_000833.5:c.547T>G	NP_000824.1:p.Phe183Val