Canonical Allele Identifier: CA394706015

Gene: GRIN2A

Linked Data

• MyVariant Identifiers: chr16:g.9857268A>G (hg19) ; chr16:g.9763411A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9763411A>G , CM000678.2:g.9763411A>G	GRCh38
NC_000016.9:g.9857268A>G , CM000678.1:g.9857268A>G	GRCh37
NC_000016.8:g.9764769A>G	NCBI36
NG_011812.1:g.424344T>C
NG_011812.2:g.424344T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.4133T>C MANE Select	ENSP00000332549.3:p.Val1378Ala
ENST00000535259.6:c.3319T>C	ENSP00000441572.3:p.Leu1107=
ENST00000636273.2:n.3383T>C
ENST00000674742.1:c.3662T>C	ENSP00000502200.1:p.Val1221Ala
ENST00000675398.1:c.*1503T>C	ENSP00000502752.1:n.*1503T>C
ENST00000330684.3:c.4133T>C	ENSP00000332549.3:p.Val1378Ala
ENST00000396573.6:c.4133T>C	ENSP00000379818.2:p.Val1378Ala
ENST00000396575.6:c.3722T>C	ENSP00000379820.3:p.Val1241Ala
ENST00000461292.3:n.3429T>C
ENST00000535259.5:c.3379T>C	ENSP00000441572.2:p.Leu1127=
ENST00000562109.5:c.3790T>C	ENSP00000454998.1:p.Leu1264=
NM_000833.4:c.4133T>C	NP_000824.1:p.Val1378Ala
NM_001134407.2:c.4133T>C	NP_001127879.1:p.Val1378Ala
NM_001134408.2:c.3790T>C	NP_001127880.1:p.Leu1264=
XM_011522456.1:c.3974T>C	XP_011520758.1:p.Val1325Ala
XM_011522457.1:c.3875T>C	XP_011520759.1:p.Val1292Ala
XM_011522458.1:c.3662T>C	XP_011520760.1:p.Val1221Ala
XM_011522459.1:c.3662T>C	XP_011520761.1:p.Val1221Ala
XM_011522460.1:c.3662T>C	XP_011520762.1:p.Val1221Ala
XM_011522461.1:c.3790T>C	XP_011520763.1:p.Leu1264=
XM_011522458.3:c.3662T>C	XP_011520760.1:p.Val1221Ala
XM_011522461.3:c.3790T>C	XP_011520763.1:p.Leu1264=
XM_017023172.1:c.4289T>C	XP_016878661.1:p.Val1430Ala
XM_017023173.1:c.3946T>C	XP_016878662.1:p.Leu1316=
NM_001134407.3:c.4133T>C MANE Select	NP_001127879.1:p.Val1378Ala
NM_000833.5:c.4133T>C	NP_000824.1:p.Val1378Ala