Canonical Allele Identifier: CA2631677358

Gene: GRIN2A

Linked Data

• gnomAD v4: 16-9840832-A-AAAAAAAAG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9840833_9840834insAAAAAAGA , CM000678.2:g.9840833_9840834insAAAAAAGA	GRCh38
NC_000016.9:g.9934690_9934691insAAAAAAGA , CM000678.1:g.9934690_9934691insAAAAAAGA	GRCh37
NC_000016.8:g.9842191_9842192insAAAAAAGA	NCBI36
NG_011812.1:g.346922_346923insCTTTTTTT
NG_011812.2:g.346922_346923insCTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.1498-33_1498-32insCTTTTTTT MANE Select	ENSP00000332549.3:n.1498-33_1498-32insCTTTTTTT
ENST00000535259.6:c.1027-33_1027-32insCTTTTTTT	ENSP00000441572.3:n.1027-33_1027-32insCTTTTTTT
ENST00000636273.2:n.1091-33_1091-32insCTTTTTTT
ENST00000674742.1:c.1027-33_1027-32insCTTTTTTT	ENSP00000502200.1:n.1027-33_1027-32insCTTTTTTT
ENST00000675189.1:n.1982-33_1982-32insCTTTTTTT
ENST00000675398.1:c.1498-33_1498-32insCTTTTTTT	ENSP00000502752.1:n.1498-33_1498-32insCTTTTTTT
ENST00000330684.3:c.1498-33_1498-32insCTTTTTTT	ENSP00000332549.3:n.1498-33_1498-32insCTTTTTTT
ENST00000396573.6:c.1498-33_1498-32insCTTTTTTT	ENSP00000379818.2:n.1498-33_1498-32insCTTTTTTT
ENST00000396575.6:c.1087-33_1087-32insCTTTTTTT	ENSP00000379820.3:n.1087-33_1087-32insCTTTTTTT
ENST00000461292.3:n.1137-33_1137-32insCTTTTTTT
ENST00000535259.5:c.1087-33_1087-32insCTTTTTTT	ENSP00000441572.2:n.1087-33_1087-32insCTTTTTTT
ENST00000562109.5:c.1498-33_1498-32insCTTTTTTT	ENSP00000454998.1:n.1498-33_1498-32insCTTTTTTT
NM_000833.4:c.1498-33_1498-32insCTTTTTTT	NP_000824.1:n.1498-33_1498-32insCTTTTTTT
NM_001134407.2:c.1498-33_1498-32insCTTTTTTT	NP_001127879.1:n.1498-33_1498-32insCTTTTTTT
NM_001134408.2:c.1498-33_1498-32insCTTTTTTT	NP_001127880.1:n.1498-33_1498-32insCTTTTTTT
XM_011522456.1:c.1339-33_1339-32insCTTTTTTT	XP_011520758.1:n.1339-33_1339-32insCTTTTTTT
XM_011522457.1:c.1240-33_1240-32insCTTTTTTT	XP_011520759.1:n.1240-33_1240-32insCTTTTTTT
XM_011522458.1:c.1027-33_1027-32insCTTTTTTT	XP_011520760.1:n.1027-33_1027-32insCTTTTTTT
XM_011522459.1:c.1027-33_1027-32insCTTTTTTT	XP_011520761.1:n.1027-33_1027-32insCTTTTTTT
XM_011522460.1:c.1027-33_1027-32insCTTTTTTT	XP_011520762.1:n.1027-33_1027-32insCTTTTTTT
XM_011522461.1:c.1498-33_1498-32insCTTTTTTT	XP_011520763.1:n.1498-33_1498-32insCTTTTTTT
XM_011522458.3:c.1027-33_1027-32insCTTTTTTT	XP_011520760.1:n.1027-33_1027-32insCTTTTTTT
XM_011522461.3:c.1498-33_1498-32insCTTTTTTT	XP_011520763.1:n.1498-33_1498-32insCTTTTTTT
XM_017023172.1:c.1654-33_1654-32insCTTTTTTT	XP_016878661.1:n.1654-33_1654-32insCTTTTTTT
XM_017023173.1:c.1654-33_1654-32insCTTTTTTT	XP_016878662.1:n.1654-33_1654-32insCTTTTTTT
NM_001134407.3:c.1498-33_1498-32insCTTTTTTT MANE Select	NP_001127879.1:n.1498-33_1498-32insCTTTTTTT
NM_000833.5:c.1498-33_1498-32insCTTTTTTT	NP_000824.1:n.1498-33_1498-32insCTTTTTTT