Canonical Allele Identifier: CA394799098

Gene: GRIN2A

Linked Data

• MyVariant Identifiers: chr16:g.10032285A>T (hg19) ; chr16:g.9938428A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9938428A>T , CM000678.2:g.9938428A>T	GRCh38
NC_000016.9:g.10032285A>T , CM000678.1:g.10032285A>T	GRCh37
NC_000016.8:g.9939786A>T	NCBI36
NG_011812.1:g.249327T>A
NG_011812.2:g.249327T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000330684.4:c.538T>A MANE Select	ENSP00000332549.3:p.Tyr180Asn
ENST00000535259.6:c.67T>A	ENSP00000441572.3:p.Tyr23Asn
ENST00000636273.2:n.131T>A
ENST00000637393.1:c.130T>A	ENSP00000490232.1:p.Tyr44Asn
ENST00000674742.1:c.67T>A	ENSP00000502200.1:p.Tyr23Asn
ENST00000675189.1:n.1022T>A
ENST00000675398.1:c.538T>A	ENSP00000502752.1:p.Tyr180Asn
ENST00000330684.3:c.538T>A	ENSP00000332549.3:p.Tyr180Asn
ENST00000396573.6:c.538T>A	ENSP00000379818.2:p.Tyr180Asn
ENST00000396575.6:c.127T>A	ENSP00000379820.3:p.Tyr43Asn
ENST00000461292.3:n.177T>A
ENST00000535259.5:c.127T>A	ENSP00000441572.2:p.Tyr43Asn
ENST00000562109.5:c.538T>A	ENSP00000454998.1:p.Tyr180Asn
ENST00000566670.2:n.380T>A
ENST00000566683.1:n.241-47328T>A
ENST00000568247.3:n.430T>A
NM_000833.4:c.538T>A	NP_000824.1:p.Tyr180Asn
NM_001134407.2:c.538T>A	NP_001127879.1:p.Tyr180Asn
NM_001134408.2:c.538T>A	NP_001127880.1:p.Tyr180Asn
XM_011522456.1:c.379T>A	XP_011520758.1:p.Tyr127Asn
XM_011522457.1:c.280T>A	XP_011520759.1:p.Tyr94Asn
XM_011522458.1:c.67T>A	XP_011520760.1:p.Tyr23Asn
XM_011522459.1:c.67T>A	XP_011520761.1:p.Tyr23Asn
XM_011522460.1:c.67T>A	XP_011520762.1:p.Tyr23Asn
XM_011522461.1:c.538T>A	XP_011520763.1:p.Tyr180Asn
XM_011522458.3:c.67T>A	XP_011520760.1:p.Tyr23Asn
XM_011522461.3:c.538T>A	XP_011520763.1:p.Tyr180Asn
XM_017023172.1:c.694T>A	XP_016878661.1:p.Tyr232Asn
XM_017023173.1:c.694T>A	XP_016878662.1:p.Tyr232Asn
NM_001134407.3:c.538T>A MANE Select	NP_001127879.1:p.Tyr180Asn
NM_000833.5:c.538T>A	NP_000824.1:p.Tyr180Asn