Canonical Allele Identifier: CA394798132

Gene: GRIN2A

Linked Data

• MyVariant Identifiers: chr16:g.10031864C>G (hg19) ; chr16:g.9938007C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9938007C>G , CM000678.2:g.9938007C>G	GRCh38
NC_000016.9:g.10031864C>G , CM000678.1:g.10031864C>G	GRCh37
NC_000016.8:g.9939365C>G	NCBI36
NG_011812.1:g.249748G>C
NG_011812.2:g.249748G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.959G>C MANE Select	ENSP00000332549.3:p.Cys320Ser
ENST00000535259.6:c.488G>C	ENSP00000441572.3:p.Cys163Ser
ENST00000636273.2:n.552G>C
ENST00000637393.1:c.551G>C	ENSP00000490232.1:p.Cys184Ser
ENST00000674742.1:c.488G>C	ENSP00000502200.1:p.Cys163Ser
ENST00000675189.1:n.1443G>C
ENST00000675398.1:c.959G>C	ENSP00000502752.1:p.Cys320Ser
ENST00000330684.3:c.959G>C	ENSP00000332549.3:p.Cys320Ser
ENST00000396573.6:c.959G>C	ENSP00000379818.2:p.Cys320Ser
ENST00000396575.6:c.548G>C	ENSP00000379820.3:p.Cys183Ser
ENST00000461292.3:n.598G>C
ENST00000535259.5:c.548G>C	ENSP00000441572.2:p.Cys183Ser
ENST00000562109.5:c.959G>C	ENSP00000454998.1:p.Cys320Ser
ENST00000566683.1:n.241-46907G>C
ENST00000568247.3:n.851G>C
NM_000833.4:c.959G>C	NP_000824.1:p.Cys320Ser
NM_001134407.2:c.959G>C	NP_001127879.1:p.Cys320Ser
NM_001134408.2:c.959G>C	NP_001127880.1:p.Cys320Ser
XM_011522456.1:c.800G>C	XP_011520758.1:p.Cys267Ser
XM_011522457.1:c.701G>C	XP_011520759.1:p.Cys234Ser
XM_011522458.1:c.488G>C	XP_011520760.1:p.Cys163Ser
XM_011522459.1:c.488G>C	XP_011520761.1:p.Cys163Ser
XM_011522460.1:c.488G>C	XP_011520762.1:p.Cys163Ser
XM_011522461.1:c.959G>C	XP_011520763.1:p.Cys320Ser
XM_011522458.3:c.488G>C	XP_011520760.1:p.Cys163Ser
XM_011522461.3:c.959G>C	XP_011520763.1:p.Cys320Ser
XM_017023172.1:c.1115G>C	XP_016878661.1:p.Cys372Ser
XM_017023173.1:c.1115G>C	XP_016878662.1:p.Cys372Ser
NM_001134407.3:c.959G>C MANE Select	NP_001127879.1:p.Cys320Ser
NM_000833.5:c.959G>C	NP_000824.1:p.Cys320Ser