Canonical Allele Identifier: CA394800418

Gene: GRIN2A

Linked Data

• dbSNP Id: rs1064796950
• MyVariant Identifiers: chr16:g.9934617G>C (hg19) ; chr16:g.9840760G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9840760G>C , CM000678.2:g.9840760G>C	GRCh38
NC_000016.9:g.9934617G>C , CM000678.1:g.9934617G>C	GRCh37
NC_000016.8:g.9842118G>C	NCBI36
NG_011812.1:g.346995C>G
NG_011812.2:g.346995C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.1538C>G MANE Select	ENSP00000332549.3:p.Thr513Ser
ENST00000535259.6:c.1067C>G	ENSP00000441572.3:p.Thr356Ser
ENST00000636273.2:n.1131C>G
ENST00000674742.1:c.1067C>G	ENSP00000502200.1:p.Thr356Ser
ENST00000675189.1:n.2022C>G
ENST00000675398.1:c.1538C>G	ENSP00000502752.1:p.Thr513Ser
ENST00000330684.3:c.1538C>G	ENSP00000332549.3:p.Thr513Ser
ENST00000396573.6:c.1538C>G	ENSP00000379818.2:p.Thr513Ser
ENST00000396575.6:c.1127C>G	ENSP00000379820.3:p.Thr376Ser
ENST00000461292.3:n.1177C>G
ENST00000535259.5:c.1127C>G	ENSP00000441572.2:p.Thr376Ser
ENST00000562109.5:c.1538C>G	ENSP00000454998.1:p.Thr513Ser
NM_000833.4:c.1538C>G	NP_000824.1:p.Thr513Ser
NM_001134407.2:c.1538C>G	NP_001127879.1:p.Thr513Ser
NM_001134408.2:c.1538C>G	NP_001127880.1:p.Thr513Ser
XM_011522456.1:c.1379C>G	XP_011520758.1:p.Thr460Ser
XM_011522457.1:c.1280C>G	XP_011520759.1:p.Thr427Ser
XM_011522458.1:c.1067C>G	XP_011520760.1:p.Thr356Ser
XM_011522459.1:c.1067C>G	XP_011520761.1:p.Thr356Ser
XM_011522460.1:c.1067C>G	XP_011520762.1:p.Thr356Ser
XM_011522461.1:c.1538C>G	XP_011520763.1:p.Thr513Ser
XM_011522458.3:c.1067C>G	XP_011520760.1:p.Thr356Ser
XM_011522461.3:c.1538C>G	XP_011520763.1:p.Thr513Ser
XM_017023172.1:c.1694C>G	XP_016878661.1:p.Thr565Ser
XM_017023173.1:c.1694C>G	XP_016878662.1:p.Thr565Ser
NM_001134407.3:c.1538C>G MANE Select	NP_001127879.1:p.Thr513Ser
NM_000833.5:c.1538C>G	NP_000824.1:p.Thr513Ser