Canonical Allele Identifier: CA2631677327

Gene: GRIN2A

Linked Data

• gnomAD v4: 16-9840814-A-AAAAAAAAAAAAAAAAAAAAAAG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9840833_9840834insAAGAAAAAAAAAAAAAAAAAAA , CM000678.2:g.9840833_9840834insAAGAAAAAAAAAAAAAAAAAAA	GRCh38
NC_000016.9:g.9934690_9934691insAAGAAAAAAAAAAAAAAAAAAA , CM000678.1:g.9934690_9934691insAAGAAAAAAAAAAAAAAAAAAA	GRCh37
NC_000016.8:g.9842191_9842192insAAGAAAAAAAAAAAAAAAAAAA	NCBI36
NG_011812.1:g.346940_346941insCTTTTTTTTTTTTTTTTTTTTT
NG_011812.2:g.346940_346941insCTTTTTTTTTTTTTTTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.1498-15_1498-14insCTTTTTTTTTTTTTTTTTTTTT MANE Select	ENSP00000332549.3:n.1498-15_1498-14insCTTTTTTTTTTTTTTTTTTTTT
ENST00000535259.6:c.1027-15_1027-14insCTTTTTTTTTTTTTTTTTTTTT	ENSP00000441572.3:n.1027-15_1027-14insCTTTTTTTTTTTTTTTTTTTTT
ENST00000636273.2:n.1091-15_1091-14insCTTTTTTTTTTTTTTTTTTTTT
ENST00000674742.1:c.1027-15_1027-14insCTTTTTTTTTTTTTTTTTTTTT	ENSP00000502200.1:n.1027-15_1027-14insCTTTTTTTTTTTTTTTTTTTTT
ENST00000675189.1:n.1982-15_1982-14insCTTTTTTTTTTTTTTTTTTTTT
ENST00000675398.1:c.1498-15_1498-14insCTTTTTTTTTTTTTTTTTTTTT	ENSP00000502752.1:n.1498-15_1498-14insCTTTTTTTTTTTTTTTTTTTTT
ENST00000330684.3:c.1498-15_1498-14insCTTTTTTTTTTTTTTTTTTTTT	ENSP00000332549.3:n.1498-15_1498-14insCTTTTTTTTTTTTTTTTTTTTT
ENST00000396573.6:c.1498-15_1498-14insCTTTTTTTTTTTTTTTTTTTTT	ENSP00000379818.2:n.1498-15_1498-14insCTTTTTTTTTTTTTTTTTTTTT
ENST00000396575.6:c.1087-15_1087-14insCTTTTTTTTTTTTTTTTTTTTT	ENSP00000379820.3:n.1087-15_1087-14insCTTTTTTTTTTTTTTTTTTTTT
ENST00000461292.3:n.1137-15_1137-14insCTTTTTTTTTTTTTTTTTTTTT
ENST00000535259.5:c.1087-15_1087-14insCTTTTTTTTTTTTTTTTTTTTT	ENSP00000441572.2:n.1087-15_1087-14insCTTTTTTTTTTTTTTTTTTTTT
ENST00000562109.5:c.1498-15_1498-14insCTTTTTTTTTTTTTTTTTTTTT	ENSP00000454998.1:n.1498-15_1498-14insCTTTTTTTTTTTTTTTTTTTTT
NM_000833.4:c.1498-15_1498-14insCTTTTTTTTTTTTTTTTTTTTT	NP_000824.1:n.1498-15_1498-14insCTTTTTTTTTTTTTTTTTTTTT
NM_001134407.2:c.1498-15_1498-14insCTTTTTTTTTTTTTTTTTTTTT	NP_001127879.1:n.1498-15_1498-14insCTTTTTTTTTTTTTTTTTTTTT
NM_001134408.2:c.1498-15_1498-14insCTTTTTTTTTTTTTTTTTTTTT	NP_001127880.1:n.1498-15_1498-14insCTTTTTTTTTTTTTTTTTTTTT
XM_011522456.1:c.1339-15_1339-14insCTTTTTTTTTTTTTTTTTTTTT	XP_011520758.1:n.1339-15_1339-14insCTTTTTTTTTTTTTTTTTTTTT
XM_011522457.1:c.1240-15_1240-14insCTTTTTTTTTTTTTTTTTTTTT	XP_011520759.1:n.1240-15_1240-14insCTTTTTTTTTTTTTTTTTTTTT
XM_011522458.1:c.1027-15_1027-14insCTTTTTTTTTTTTTTTTTTTTT	XP_011520760.1:n.1027-15_1027-14insCTTTTTTTTTTTTTTTTTTTTT
XM_011522459.1:c.1027-15_1027-14insCTTTTTTTTTTTTTTTTTTTTT	XP_011520761.1:n.1027-15_1027-14insCTTTTTTTTTTTTTTTTTTTTT
XM_011522460.1:c.1027-15_1027-14insCTTTTTTTTTTTTTTTTTTTTT	XP_011520762.1:n.1027-15_1027-14insCTTTTTTTTTTTTTTTTTTTTT
XM_011522461.1:c.1498-15_1498-14insCTTTTTTTTTTTTTTTTTTTTT	XP_011520763.1:n.1498-15_1498-14insCTTTTTTTTTTTTTTTTTTTTT
XM_011522458.3:c.1027-15_1027-14insCTTTTTTTTTTTTTTTTTTTTT	XP_011520760.1:n.1027-15_1027-14insCTTTTTTTTTTTTTTTTTTTTT
XM_011522461.3:c.1498-15_1498-14insCTTTTTTTTTTTTTTTTTTTTT	XP_011520763.1:n.1498-15_1498-14insCTTTTTTTTTTTTTTTTTTTTT
XM_017023172.1:c.1654-15_1654-14insCTTTTTTTTTTTTTTTTTTTTT	XP_016878661.1:n.1654-15_1654-14insCTTTTTTTTTTTTTTTTTTTTT
XM_017023173.1:c.1654-15_1654-14insCTTTTTTTTTTTTTTTTTTTTT	XP_016878662.1:n.1654-15_1654-14insCTTTTTTTTTTTTTTTTTTTTT
NM_001134407.3:c.1498-15_1498-14insCTTTTTTTTTTTTTTTTTTTTT MANE Select	NP_001127879.1:n.1498-15_1498-14insCTTTTTTTTTTTTTTTTTTTTT
NM_000833.5:c.1498-15_1498-14insCTTTTTTTTTTTTTTTTTTTTT	NP_000824.1:n.1498-15_1498-14insCTTTTTTTTTTTTTTTTTTTTT