Canonical Allele Identifier: CA493702302

Gene: GRIN2A

Linked Data

• MyVariant Identifiers: chr16:g.10032214C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9938357C>A , CM000678.2:g.9938357C>A	GRCh38
NC_000016.9:g.10032214C>A , CM000678.1:g.10032214C>A	GRCh37
NC_000016.8:g.9939715C>A	NCBI36
NG_011812.1:g.249398G>T
NG_011812.2:g.249398G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.609G>T MANE Select	ENSP00000332549.3:p.Val203=
ENST00000535259.6:c.138G>T	ENSP00000441572.3:p.Val46=
ENST00000636273.2:n.202G>T
ENST00000637393.1:c.201G>T	ENSP00000490232.1:p.Val67=
ENST00000674742.1:c.138G>T	ENSP00000502200.1:p.Val46=
ENST00000675189.1:n.1093G>T
ENST00000675398.1:c.609G>T	ENSP00000502752.1:p.Val203=
ENST00000330684.3:c.609G>T	ENSP00000332549.3:p.Val203=
ENST00000396573.6:c.609G>T	ENSP00000379818.2:p.Val203=
ENST00000396575.6:c.198G>T	ENSP00000379820.3:p.Val66=
ENST00000461292.3:n.248G>T
ENST00000535259.5:c.198G>T	ENSP00000441572.2:p.Val66=
ENST00000562109.5:c.609G>T	ENSP00000454998.1:p.Val203=
ENST00000566670.2:n.451G>T
ENST00000566683.1:n.241-47257G>T
ENST00000568247.3:n.501G>T
NM_000833.4:c.609G>T	NP_000824.1:p.Val203=
NM_001134407.2:c.609G>T	NP_001127879.1:p.Val203=
NM_001134408.2:c.609G>T	NP_001127880.1:p.Val203=
XM_011522456.1:c.450G>T	XP_011520758.1:p.Val150=
XM_011522457.1:c.351G>T	XP_011520759.1:p.Val117=
XM_011522458.1:c.138G>T	XP_011520760.1:p.Val46=
XM_011522459.1:c.138G>T	XP_011520761.1:p.Val46=
XM_011522460.1:c.138G>T	XP_011520762.1:p.Val46=
XM_011522461.1:c.609G>T	XP_011520763.1:p.Val203=
XM_011522458.3:c.138G>T	XP_011520760.1:p.Val46=
XM_011522461.3:c.609G>T	XP_011520763.1:p.Val203=
XM_017023172.1:c.765G>T	XP_016878661.1:p.Val255=
XM_017023173.1:c.765G>T	XP_016878662.1:p.Val255=
NM_001134407.3:c.609G>T MANE Select	NP_001127879.1:p.Val203=
NM_000833.5:c.609G>T	NP_000824.1:p.Val203=