Canonical Allele Identifier: CA2695201990

Gene: GRIN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9840832_9840834delinsAAG , CM000678.2:g.9840832_9840834delinsAAG	GRCh38
NC_000016.9:g.9934689_9934691delinsAAG , CM000678.1:g.9934689_9934691delinsAAG	GRCh37
NC_000016.8:g.9842190_9842192delinsAAG	NCBI36
NG_011812.1:g.346921_346923delinsCTT
NG_011812.2:g.346921_346923delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.1498-34_1498-32delinsCTT MANE Select	ENSP00000332549.3:n.1498-34_1498-32delinsCTT
ENST00000535259.6:c.1027-34_1027-32delinsCTT	ENSP00000441572.3:n.1027-34_1027-32delinsCTT
ENST00000636273.2:n.1091-34_1091-32delinsCTT
ENST00000674742.1:c.1027-34_1027-32delinsCTT	ENSP00000502200.1:n.1027-34_1027-32delinsCTT
ENST00000675189.1:n.1982-34_1982-32delinsCTT
ENST00000675398.1:c.1498-34_1498-32delinsCTT	ENSP00000502752.1:n.1498-34_1498-32delinsCTT
ENST00000330684.3:c.1498-34_1498-32delinsCTT	ENSP00000332549.3:n.1498-34_1498-32delinsCTT
ENST00000396573.6:c.1498-34_1498-32delinsCTT	ENSP00000379818.2:n.1498-34_1498-32delinsCTT
ENST00000396575.6:c.1087-34_1087-32delinsCTT	ENSP00000379820.3:n.1087-34_1087-32delinsCTT
ENST00000461292.3:n.1137-34_1137-32delinsCTT
ENST00000535259.5:c.1087-34_1087-32delinsCTT	ENSP00000441572.2:n.1087-34_1087-32delinsCTT
ENST00000562109.5:c.1498-34_1498-32delinsCTT	ENSP00000454998.1:n.1498-34_1498-32delinsCTT
NM_000833.4:c.1498-34_1498-32delinsCTT	NP_000824.1:n.1498-34_1498-32delinsCTT
NM_001134407.2:c.1498-34_1498-32delinsCTT	NP_001127879.1:n.1498-34_1498-32delinsCTT
NM_001134408.2:c.1498-34_1498-32delinsCTT	NP_001127880.1:n.1498-34_1498-32delinsCTT
XM_011522456.1:c.1339-34_1339-32delinsCTT	XP_011520758.1:n.1339-34_1339-32delinsCTT
XM_011522457.1:c.1240-34_1240-32delinsCTT	XP_011520759.1:n.1240-34_1240-32delinsCTT
XM_011522458.1:c.1027-34_1027-32delinsCTT	XP_011520760.1:n.1027-34_1027-32delinsCTT
XM_011522459.1:c.1027-34_1027-32delinsCTT	XP_011520761.1:n.1027-34_1027-32delinsCTT
XM_011522460.1:c.1027-34_1027-32delinsCTT	XP_011520762.1:n.1027-34_1027-32delinsCTT
XM_011522461.1:c.1498-34_1498-32delinsCTT	XP_011520763.1:n.1498-34_1498-32delinsCTT
XM_011522458.3:c.1027-34_1027-32delinsCTT	XP_011520760.1:n.1027-34_1027-32delinsCTT
XM_011522461.3:c.1498-34_1498-32delinsCTT	XP_011520763.1:n.1498-34_1498-32delinsCTT
XM_017023172.1:c.1654-34_1654-32delinsCTT	XP_016878661.1:n.1654-34_1654-32delinsCTT
XM_017023173.1:c.1654-34_1654-32delinsCTT	XP_016878662.1:n.1654-34_1654-32delinsCTT
NM_001134407.3:c.1498-34_1498-32delinsCTT MANE Select	NP_001127879.1:n.1498-34_1498-32delinsCTT
NM_000833.5:c.1498-34_1498-32delinsCTT	NP_000824.1:n.1498-34_1498-32delinsCTT