Canonical Allele Identifier: CA7896415

Gene: GRIN2A

Linked Data

• dbSNP Id: rs772385154
• ExAC: 16:9858578 C / A
• gnomAD v3: 16-9764721-C-A
• gnomAD v4: 16-9764721-C-A
• MyVariant Identifiers: chr16:g.9858578C>A (hg19) ; chr16:g.9764721C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9764721C>A , CM000678.2:g.9764721C>A	GRCh38
NC_000016.9:g.9858578C>A , CM000678.1:g.9858578C>A	GRCh37
NC_000016.8:g.9766079C>A	NCBI36
NG_011812.1:g.423034G>T
NG_011812.2:g.423034G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000330684.4:c.2823G>T MANE Select	ENSP00000332549.3:p.Leu941Phe
ENST00000535259.6:c.2352G>T	ENSP00000441572.3:p.Leu784Phe
ENST00000636273.2:n.2416G>T
ENST00000674742.1:c.2352G>T	ENSP00000502200.1:p.Leu784Phe
ENST00000675398.1:c.*193G>T	ENSP00000502752.1:n.*193G>T
ENST00000330684.3:c.2823G>T	ENSP00000332549.3:p.Leu941Phe
ENST00000396573.6:c.2823G>T	ENSP00000379818.2:p.Leu941Phe
ENST00000396575.6:c.2412G>T	ENSP00000379820.3:p.Leu804Phe
ENST00000461292.3:n.2462G>T
ENST00000535259.5:c.2412G>T	ENSP00000441572.2:p.Leu804Phe
ENST00000562109.5:c.2823G>T	ENSP00000454998.1:p.Leu941Phe
NM_000833.4:c.2823G>T	NP_000824.1:p.Leu941Phe
NM_001134407.2:c.2823G>T	NP_001127879.1:p.Leu941Phe
NM_001134408.2:c.2823G>T	NP_001127880.1:p.Leu941Phe
XM_011522456.1:c.2664G>T	XP_011520758.1:p.Leu888Phe
XM_011522457.1:c.2565G>T	XP_011520759.1:p.Leu855Phe
XM_011522458.1:c.2352G>T	XP_011520760.1:p.Leu784Phe
XM_011522459.1:c.2352G>T	XP_011520761.1:p.Leu784Phe
XM_011522460.1:c.2352G>T	XP_011520762.1:p.Leu784Phe
XM_011522461.1:c.2823G>T	XP_011520763.1:p.Leu941Phe
XM_011522458.3:c.2352G>T	XP_011520760.1:p.Leu784Phe
XM_011522461.3:c.2823G>T	XP_011520763.1:p.Leu941Phe
XM_017023172.1:c.2979G>T	XP_016878661.1:p.Leu993Phe
XM_017023173.1:c.2979G>T	XP_016878662.1:p.Leu993Phe
NM_001134407.3:c.2823G>T MANE Select	NP_001127879.1:p.Leu941Phe
NM_000833.5:c.2823G>T	NP_000824.1:p.Leu941Phe