Canonical Allele Identifier: CA493683150

Gene: GRIN2A

Linked Data

• MyVariant Identifiers: chr16:g.10031938G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9938081G>T , CM000678.2:g.9938081G>T	GRCh38
NC_000016.9:g.10031938G>T , CM000678.1:g.10031938G>T	GRCh37
NC_000016.8:g.9939439G>T	NCBI36
NG_011812.1:g.249674C>A
NG_011812.2:g.249674C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.885C>A MANE Select	ENSP00000332549.3:p.Gly295=
ENST00000535259.6:c.414C>A	ENSP00000441572.3:p.Gly138=
ENST00000636273.2:n.478C>A
ENST00000637393.1:c.477C>A	ENSP00000490232.1:p.Gly159=
ENST00000674742.1:c.414C>A	ENSP00000502200.1:p.Gly138=
ENST00000675189.1:n.1369C>A
ENST00000675398.1:c.885C>A	ENSP00000502752.1:p.Gly295=
ENST00000330684.3:c.885C>A	ENSP00000332549.3:p.Gly295=
ENST00000396573.6:c.885C>A	ENSP00000379818.2:p.Gly295=
ENST00000396575.6:c.474C>A	ENSP00000379820.3:p.Gly158=
ENST00000461292.3:n.524C>A
ENST00000535259.5:c.474C>A	ENSP00000441572.2:p.Gly158=
ENST00000562109.5:c.885C>A	ENSP00000454998.1:p.Gly295=
ENST00000566683.1:n.241-46981C>A
ENST00000568247.3:n.777C>A
NM_000833.4:c.885C>A	NP_000824.1:p.Gly295=
NM_001134407.2:c.885C>A	NP_001127879.1:p.Gly295=
NM_001134408.2:c.885C>A	NP_001127880.1:p.Gly295=
XM_011522456.1:c.726C>A	XP_011520758.1:p.Gly242=
XM_011522457.1:c.627C>A	XP_011520759.1:p.Gly209=
XM_011522458.1:c.414C>A	XP_011520760.1:p.Gly138=
XM_011522459.1:c.414C>A	XP_011520761.1:p.Gly138=
XM_011522460.1:c.414C>A	XP_011520762.1:p.Gly138=
XM_011522461.1:c.885C>A	XP_011520763.1:p.Gly295=
XM_011522458.3:c.414C>A	XP_011520760.1:p.Gly138=
XM_011522461.3:c.885C>A	XP_011520763.1:p.Gly295=
XM_017023172.1:c.1041C>A	XP_016878661.1:p.Gly347=
XM_017023173.1:c.1041C>A	XP_016878662.1:p.Gly347=
NM_001134407.3:c.885C>A MANE Select	NP_001127879.1:p.Gly295=
NM_000833.5:c.885C>A	NP_000824.1:p.Gly295=