Canonical Allele Identifier: CA394798914

Gene: GRIN2A

Linked Data

• MyVariant Identifiers: chr16:g.10032224A>G (hg19) ; chr16:g.9938367A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9938367A>G , CM000678.2:g.9938367A>G	GRCh38
NC_000016.9:g.10032224A>G , CM000678.1:g.10032224A>G	GRCh37
NC_000016.8:g.9939725A>G	NCBI36
NG_011812.1:g.249388T>C
NG_011812.2:g.249388T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.599T>C MANE Select	ENSP00000332549.3:p.Met200Thr
ENST00000535259.6:c.128T>C	ENSP00000441572.3:p.Met43Thr
ENST00000636273.2:n.192T>C
ENST00000637393.1:c.191T>C	ENSP00000490232.1:p.Met64Thr
ENST00000674742.1:c.128T>C	ENSP00000502200.1:p.Met43Thr
ENST00000675189.1:n.1083T>C
ENST00000675398.1:c.599T>C	ENSP00000502752.1:p.Met200Thr
ENST00000330684.3:c.599T>C	ENSP00000332549.3:p.Met200Thr
ENST00000396573.6:c.599T>C	ENSP00000379818.2:p.Met200Thr
ENST00000396575.6:c.188T>C	ENSP00000379820.3:p.Met63Thr
ENST00000461292.3:n.238T>C
ENST00000535259.5:c.188T>C	ENSP00000441572.2:p.Met63Thr
ENST00000562109.5:c.599T>C	ENSP00000454998.1:p.Met200Thr
ENST00000566670.2:n.441T>C
ENST00000566683.1:n.241-47267T>C
ENST00000568247.3:n.491T>C
NM_000833.4:c.599T>C	NP_000824.1:p.Met200Thr
NM_001134407.2:c.599T>C	NP_001127879.1:p.Met200Thr
NM_001134408.2:c.599T>C	NP_001127880.1:p.Met200Thr
XM_011522456.1:c.440T>C	XP_011520758.1:p.Met147Thr
XM_011522457.1:c.341T>C	XP_011520759.1:p.Met114Thr
XM_011522458.1:c.128T>C	XP_011520760.1:p.Met43Thr
XM_011522459.1:c.128T>C	XP_011520761.1:p.Met43Thr
XM_011522460.1:c.128T>C	XP_011520762.1:p.Met43Thr
XM_011522461.1:c.599T>C	XP_011520763.1:p.Met200Thr
XM_011522458.3:c.128T>C	XP_011520760.1:p.Met43Thr
XM_011522461.3:c.599T>C	XP_011520763.1:p.Met200Thr
XM_017023172.1:c.755T>C	XP_016878661.1:p.Met252Thr
XM_017023173.1:c.755T>C	XP_016878662.1:p.Met252Thr
NM_001134407.3:c.599T>C MANE Select	NP_001127879.1:p.Met200Thr
NM_000833.5:c.599T>C	NP_000824.1:p.Met200Thr