Canonical Allele Identifier: CA2206732633

Gene: GRIN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9840656_9840659delinsCAGA , CM000678.2:g.9840656_9840659delinsCAGA	GRCh38
NC_000016.9:g.9934513_9934516delinsCAGA , CM000678.1:g.9934513_9934516delinsCAGA	GRCh37
NC_000016.8:g.9842014_9842017delinsCAGA	NCBI36
NG_011812.1:g.347096_347099delinsTCTG
NG_011812.2:g.347096_347099delinsTCTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000330684.4:c.1639_1642delinsTCTG MANE Select	ENSP00000332549.3:p.Ser547=
ENST00000535259.6:c.1168_1171delinsTCTG	ENSP00000441572.3:p.Ser390=
ENST00000636273.2:n.1232_1235delinsTCTG
ENST00000674742.1:c.1168_1171delinsTCTG	ENSP00000502200.1:p.Ser390=
ENST00000675189.1:n.2123_2126delinsTCTG
ENST00000675398.1:c.1639_1642delinsTCTG	ENSP00000502752.1:p.Ser547=
ENST00000330684.3:c.1639_1642delinsTCTG	ENSP00000332549.3:p.Ser547=
ENST00000396573.6:c.1639_1642delinsTCTG	ENSP00000379818.2:p.Ser547=
ENST00000396575.6:c.1228_1231delinsTCTG	ENSP00000379820.3:p.Ser410=
ENST00000461292.3:n.1278_1281delinsTCTG
ENST00000535259.5:c.1228_1231delinsTCTG	ENSP00000441572.2:p.Ser410=
ENST00000562109.5:c.1639_1642delinsTCTG	ENSP00000454998.1:p.Ser547=
NM_000833.4:c.1639_1642delinsTCTG	NP_000824.1:p.Ser547=
NM_001134407.2:c.1639_1642delinsTCTG	NP_001127879.1:p.Ser547=
NM_001134408.2:c.1639_1642delinsTCTG	NP_001127880.1:p.Ser547=
XM_011522456.1:c.1480_1483delinsTCTG	XP_011520758.1:p.Ser494=
XM_011522457.1:c.1381_1384delinsTCTG	XP_011520759.1:p.Ser461=
XM_011522458.1:c.1168_1171delinsTCTG	XP_011520760.1:p.Ser390=
XM_011522459.1:c.1168_1171delinsTCTG	XP_011520761.1:p.Ser390=
XM_011522460.1:c.1168_1171delinsTCTG	XP_011520762.1:p.Ser390=
XM_011522461.1:c.1639_1642delinsTCTG	XP_011520763.1:p.Ser547=
XM_011522458.3:c.1168_1171delinsTCTG	XP_011520760.1:p.Ser390=
XM_011522461.3:c.1639_1642delinsTCTG	XP_011520763.1:p.Ser547=
XM_017023172.1:c.1795_1798delinsTCTG	XP_016878661.1:p.Ser599=
XM_017023173.1:c.1795_1798delinsTCTG	XP_016878662.1:p.Ser599=
NM_001134407.3:c.1639_1642delinsTCTG MANE Select	NP_001127879.1:p.Ser547=
NM_000833.5:c.1639_1642delinsTCTG	NP_000824.1:p.Ser547=