Canonical Allele Identifier: CA394797299

Gene: GRIN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9798442C>A , CM000678.2:g.9798442C>A	GRCh38
NC_000016.9:g.9892299C>A , CM000678.1:g.9892299C>A	GRCh37
NC_000016.8:g.9799800C>A	NCBI36
NG_011812.1:g.389313G>T
NG_011812.2:g.389313G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.2191G>T MANE Select	ENSP00000332549.3:p.Asp731Tyr
ENST00000535259.6:c.1720G>T	ENSP00000441572.3:p.Asp574Tyr
ENST00000636273.2:n.1784G>T
ENST00000674742.1:c.1720G>T	ENSP00000502200.1:p.Asp574Tyr
ENST00000675398.1:c.2191G>T	ENSP00000502752.1:p.Asp731Tyr
ENST00000330684.3:c.2191G>T	ENSP00000332549.3:p.Asp731Tyr
ENST00000396573.6:c.2191G>T	ENSP00000379818.2:p.Asp731Tyr
ENST00000396575.6:c.1780G>T	ENSP00000379820.3:p.Asp594Tyr
ENST00000461292.3:n.1830G>T
ENST00000535259.5:c.1780G>T	ENSP00000441572.2:p.Asp594Tyr
ENST00000562109.5:c.2191G>T	ENSP00000454998.1:p.Asp731Tyr
NM_000833.4:c.2191G>T	NP_000824.1:p.Asp731Tyr
NM_001134407.2:c.2191G>T	NP_001127879.1:p.Asp731Tyr
NM_001134408.2:c.2191G>T	NP_001127880.1:p.Asp731Tyr
XM_011522456.1:c.2032G>T	XP_011520758.1:p.Asp678Tyr
XM_011522457.1:c.1933G>T	XP_011520759.1:p.Asp645Tyr
XM_011522458.1:c.1720G>T	XP_011520760.1:p.Asp574Tyr
XM_011522459.1:c.1720G>T	XP_011520761.1:p.Asp574Tyr
XM_011522460.1:c.1720G>T	XP_011520762.1:p.Asp574Tyr
XM_011522461.1:c.2191G>T	XP_011520763.1:p.Asp731Tyr
XR_933062.1:n.300+3720C>A
XR_933063.1:n.300+3720C>A
XM_011522458.3:c.1720G>T	XP_011520760.1:p.Asp574Tyr
XM_011522461.3:c.2191G>T	XP_011520763.1:p.Asp731Tyr
XM_017023172.1:c.2347G>T	XP_016878661.1:p.Asp783Tyr
XM_017023173.1:c.2347G>T	XP_016878662.1:p.Asp783Tyr
XR_933062.3:n.3304+3720C>A
XR_933063.3:n.3304+3720C>A
NM_001134407.3:c.2191G>T MANE Select	NP_001127879.1:p.Asp731Tyr
NM_000833.5:c.2191G>T	NP_000824.1:p.Asp731Tyr