Canonical Allele Identifier: CA394798126

Gene: GRIN2A

Linked Data

• MyVariant Identifiers: chr16:g.10031862A>C (hg19) ; chr16:g.9938005A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9938005A>C , CM000678.2:g.9938005A>C	GRCh38
NC_000016.9:g.10031862A>C , CM000678.1:g.10031862A>C	GRCh37
NC_000016.8:g.9939363A>C	NCBI36
NG_011812.1:g.249750T>G
NG_011812.2:g.249750T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.961T>G MANE Select	ENSP00000332549.3:p.Tyr321Asp
ENST00000535259.6:c.490T>G	ENSP00000441572.3:p.Tyr164Asp
ENST00000636273.2:n.554T>G
ENST00000637393.1:c.553T>G	ENSP00000490232.1:p.Tyr185Asp
ENST00000674742.1:c.490T>G	ENSP00000502200.1:p.Tyr164Asp
ENST00000675189.1:n.1445T>G
ENST00000675398.1:c.961T>G	ENSP00000502752.1:p.Tyr321Asp
ENST00000330684.3:c.961T>G	ENSP00000332549.3:p.Tyr321Asp
ENST00000396573.6:c.961T>G	ENSP00000379818.2:p.Tyr321Asp
ENST00000396575.6:c.550T>G	ENSP00000379820.3:p.Tyr184Asp
ENST00000461292.3:n.600T>G
ENST00000535259.5:c.550T>G	ENSP00000441572.2:p.Tyr184Asp
ENST00000562109.5:c.961T>G	ENSP00000454998.1:p.Tyr321Asp
ENST00000566683.1:n.241-46905T>G
ENST00000568247.3:n.853T>G
NM_000833.4:c.961T>G	NP_000824.1:p.Tyr321Asp
NM_001134407.2:c.961T>G	NP_001127879.1:p.Tyr321Asp
NM_001134408.2:c.961T>G	NP_001127880.1:p.Tyr321Asp
XM_011522456.1:c.802T>G	XP_011520758.1:p.Tyr268Asp
XM_011522457.1:c.703T>G	XP_011520759.1:p.Tyr235Asp
XM_011522458.1:c.490T>G	XP_011520760.1:p.Tyr164Asp
XM_011522459.1:c.490T>G	XP_011520761.1:p.Tyr164Asp
XM_011522460.1:c.490T>G	XP_011520762.1:p.Tyr164Asp
XM_011522461.1:c.961T>G	XP_011520763.1:p.Tyr321Asp
XM_011522458.3:c.490T>G	XP_011520760.1:p.Tyr164Asp
XM_011522461.3:c.961T>G	XP_011520763.1:p.Tyr321Asp
XM_017023172.1:c.1117T>G	XP_016878661.1:p.Tyr373Asp
XM_017023173.1:c.1117T>G	XP_016878662.1:p.Tyr373Asp
NM_001134407.3:c.961T>G MANE Select	NP_001127879.1:p.Tyr321Asp
NM_000833.5:c.961T>G	NP_000824.1:p.Tyr321Asp