Canonical Allele Identifier: CA493692776

Gene: GRIN2A

Linked Data

• dbSNP Id: rs2141127347
• MyVariant Identifiers: chr16:g.9857372A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9763515A>G , CM000678.2:g.9763515A>G	GRCh38
NC_000016.9:g.9857372A>G , CM000678.1:g.9857372A>G	GRCh37
NC_000016.8:g.9764873A>G	NCBI36
NG_011812.1:g.424240T>C
NG_011812.2:g.424240T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.4029T>C MANE Select	ENSP00000332549.3:p.Leu1343=
ENST00000535259.6:c.3302-87T>C	ENSP00000441572.3:n.3302-87T>C
ENST00000636273.2:n.3366-87T>C
ENST00000674742.1:c.3558T>C	ENSP00000502200.1:p.Leu1186=
ENST00000675398.1:c.*1399T>C	ENSP00000502752.1:n.*1399T>C
ENST00000330684.3:c.4029T>C	ENSP00000332549.3:p.Leu1343=
ENST00000396573.6:c.4029T>C	ENSP00000379818.2:p.Leu1343=
ENST00000396575.6:c.3618T>C	ENSP00000379820.3:p.Leu1206=
ENST00000461292.3:n.3412-87T>C
ENST00000535259.5:c.3362-87T>C	ENSP00000441572.2:n.3362-87T>C
ENST00000562109.5:c.3773-87T>C	ENSP00000454998.1:n.3773-87T>C
NM_000833.4:c.4029T>C	NP_000824.1:p.Leu1343=
NM_001134407.2:c.4029T>C	NP_001127879.1:p.Leu1343=
NM_001134408.2:c.3773-87T>C	NP_001127880.1:n.3773-87T>C
XM_011522456.1:c.3870T>C	XP_011520758.1:p.Leu1290=
XM_011522457.1:c.3771T>C	XP_011520759.1:p.Leu1257=
XM_011522458.1:c.3558T>C	XP_011520760.1:p.Leu1186=
XM_011522459.1:c.3558T>C	XP_011520761.1:p.Leu1186=
XM_011522460.1:c.3558T>C	XP_011520762.1:p.Leu1186=
XM_011522461.1:c.3773-87T>C	XP_011520763.1:n.3773-87T>C
XM_011522458.3:c.3558T>C	XP_011520760.1:p.Leu1186=
XM_011522461.3:c.3773-87T>C	XP_011520763.1:n.3773-87T>C
XM_017023172.1:c.4185T>C	XP_016878661.1:p.Leu1395=
XM_017023173.1:c.3929-87T>C	XP_016878662.1:n.3929-87T>C
NM_001134407.3:c.4029T>C MANE Select	NP_001127879.1:p.Leu1343=
NM_000833.5:c.4029T>C	NP_000824.1:p.Leu1343=