Canonical Allele Identifier: CA394705951

Gene: GRIN2A

Linked Data

• dbSNP Id: rs2141126047
• MyVariant Identifiers: chr16:g.9857243A>G (hg19) ; chr16:g.9763386A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9763386A>G , CM000678.2:g.9763386A>G	GRCh38
NC_000016.9:g.9857243A>G , CM000678.1:g.9857243A>G	GRCh37
NC_000016.8:g.9764744A>G	NCBI36
NG_011812.1:g.424369T>C
NG_011812.2:g.424369T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.4158T>C MANE Select	ENSP00000332549.3:p.Pro1386=
ENST00000535259.6:c.3344T>C	ENSP00000441572.3:p.Leu1115Pro
ENST00000636273.2:n.3408T>C
ENST00000674742.1:c.3687T>C	ENSP00000502200.1:p.Pro1229=
ENST00000675398.1:c.*1528T>C	ENSP00000502752.1:n.*1528T>C
ENST00000330684.3:c.4158T>C	ENSP00000332549.3:p.Pro1386=
ENST00000396573.6:c.4158T>C	ENSP00000379818.2:p.Pro1386=
ENST00000396575.6:c.3747T>C	ENSP00000379820.3:p.Pro1249=
ENST00000461292.3:n.3454T>C
ENST00000535259.5:c.3404T>C	ENSP00000441572.2:p.Leu1135Pro
ENST00000562109.5:c.3815T>C	ENSP00000454998.1:p.Leu1272Pro
NM_000833.4:c.4158T>C	NP_000824.1:p.Pro1386=
NM_001134407.2:c.4158T>C	NP_001127879.1:p.Pro1386=
NM_001134408.2:c.3815T>C	NP_001127880.1:p.Leu1272Pro
XM_011522456.1:c.3999T>C	XP_011520758.1:p.Pro1333=
XM_011522457.1:c.3900T>C	XP_011520759.1:p.Pro1300=
XM_011522458.1:c.3687T>C	XP_011520760.1:p.Pro1229=
XM_011522459.1:c.3687T>C	XP_011520761.1:p.Pro1229=
XM_011522460.1:c.3687T>C	XP_011520762.1:p.Pro1229=
XM_011522461.1:c.3815T>C	XP_011520763.1:p.Leu1272Pro
XM_011522458.3:c.3687T>C	XP_011520760.1:p.Pro1229=
XM_011522461.3:c.3815T>C	XP_011520763.1:p.Leu1272Pro
XM_017023172.1:c.4314T>C	XP_016878661.1:p.Pro1438=
XM_017023173.1:c.3971T>C	XP_016878662.1:p.Leu1324Pro
NM_001134407.3:c.4158T>C MANE Select	NP_001127879.1:p.Pro1386=
NM_000833.5:c.4158T>C	NP_000824.1:p.Pro1386=