Canonical Allele Identifier: CA7896702

Gene: GRIN2A

Linked Data

• dbSNP Id: rs111268758
• ExAC: 16:9934689 AAGAG / A
• gnomAD v2: 16-9934689-AAGAG-A
• gnomAD v3: 16-9840832-AAGAG-A
• gnomAD v4: 16-9840832-AAGAG-A
• MyVariant Identifiers: chr16:g.9934692_9934695del (hg19) ; chr16:g.9934690_9934693del (hg19) ; chr16:g.9840833_9840836del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9840842_9840845del , CM000678.2:g.9840842_9840845del	GRCh38
NC_000016.9:g.9934699_9934702del , CM000678.1:g.9934699_9934702del	GRCh37
NC_000016.8:g.9842200_9842203del	NCBI36
NG_011812.1:g.346919_346922del
NG_011812.2:g.346919_346922del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.1498-36_1498-33del MANE Select	ENSP00000332549.3:n.1498-36_1498-33del
ENST00000535259.6:c.1027-36_1027-33del	ENSP00000441572.3:n.1027-36_1027-33del
ENST00000636273.2:n.1091-36_1091-33del
ENST00000674742.1:c.1027-36_1027-33del	ENSP00000502200.1:n.1027-36_1027-33del
ENST00000675189.1:n.1982-36_1982-33del
ENST00000675398.1:c.1498-36_1498-33del	ENSP00000502752.1:n.1498-36_1498-33del
ENST00000330684.3:c.1498-36_1498-33del	ENSP00000332549.3:n.1498-36_1498-33del
ENST00000396573.6:c.1498-36_1498-33del	ENSP00000379818.2:n.1498-36_1498-33del
ENST00000396575.6:c.1087-36_1087-33del	ENSP00000379820.3:n.1087-36_1087-33del
ENST00000461292.3:n.1137-36_1137-33del
ENST00000535259.5:c.1087-36_1087-33del	ENSP00000441572.2:n.1087-36_1087-33del
ENST00000562109.5:c.1498-36_1498-33del	ENSP00000454998.1:n.1498-36_1498-33del
NM_000833.4:c.1498-36_1498-33del	NP_000824.1:n.1498-36_1498-33del
NM_001134407.2:c.1498-36_1498-33del	NP_001127879.1:n.1498-36_1498-33del
NM_001134408.2:c.1498-36_1498-33del	NP_001127880.1:n.1498-36_1498-33del
XM_011522456.1:c.1339-36_1339-33del	XP_011520758.1:n.1339-36_1339-33del
XM_011522457.1:c.1240-36_1240-33del	XP_011520759.1:n.1240-36_1240-33del
XM_011522458.1:c.1027-36_1027-33del	XP_011520760.1:n.1027-36_1027-33del
XM_011522459.1:c.1027-36_1027-33del	XP_011520761.1:n.1027-36_1027-33del
XM_011522460.1:c.1027-36_1027-33del	XP_011520762.1:n.1027-36_1027-33del
XM_011522461.1:c.1498-36_1498-33del	XP_011520763.1:n.1498-36_1498-33del
XM_011522458.3:c.1027-36_1027-33del	XP_011520760.1:n.1027-36_1027-33del
XM_011522461.3:c.1498-36_1498-33del	XP_011520763.1:n.1498-36_1498-33del
XM_017023172.1:c.1654-36_1654-33del	XP_016878661.1:n.1654-36_1654-33del
XM_017023173.1:c.1654-36_1654-33del	XP_016878662.1:n.1654-36_1654-33del
NM_001134407.3:c.1498-36_1498-33del MANE Select	NP_001127879.1:n.1498-36_1498-33del
NM_000833.5:c.1498-36_1498-33del	NP_000824.1:n.1498-36_1498-33del