Canonical Allele Identifier: CA621175117

Gene: GRIN2A

Linked Data

• dbSNP Id: rs1567274965
• gnomAD v2: 16-9857088-ATAT-A
• gnomAD v4: 16-9763231-ATAT-A
• MyVariant Identifiers: chr16:g.9857089_9857091del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9763236_9763238del , CM000678.2:g.9763236_9763238del	GRCh38
NC_000016.9:g.9857093_9857095del , CM000678.1:g.9857093_9857095del	GRCh37
NC_000016.8:g.9764594_9764596del	NCBI36
NG_011812.1:g.424521_424523del
NG_011812.2:g.424521_424523del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.4310_4312del MANE Select	ENSP00000332549.3:p.Asn1437del
ENST00000535259.6:c.*121_*123del	ENSP00000441572.3:n.*121_*123del
ENST00000636273.2:n.3560_3562del
ENST00000674742.1:c.3839_3841del	ENSP00000502200.1:p.Asn1280del
ENST00000675398.1:c.*1680_*1682del	ENSP00000502752.1:n.*1680_*1682del
ENST00000330684.3:c.4310_4312del	ENSP00000332549.3:p.Asn1437del
ENST00000396573.6:c.4310_4312del	ENSP00000379818.2:p.Asn1437del
ENST00000396575.6:c.3899_3901del	ENSP00000379820.3:p.Asn1300del
ENST00000461292.3:n.3606_3608del
ENST00000535259.5:c.*121_*123del	ENSP00000441572.2:n.*121_*123del
ENST00000562109.5:c.*121_*123del	ENSP00000454998.1:n.*121_*123del
NM_000833.4:c.4310_4312del	NP_000824.1:p.Asn1437del
NM_001134407.2:c.4310_4312del	NP_001127879.1:p.Asn1437del
NM_001134408.2:c.*121_*123del	NP_001127880.1:n.*121_*123del
XM_011522456.1:c.4151_4153del	XP_011520758.1:p.Asn1384del
XM_011522457.1:c.4052_4054del	XP_011520759.1:p.Asn1351del
XM_011522458.1:c.3839_3841del	XP_011520760.1:p.Asn1280del
XM_011522459.1:c.3839_3841del	XP_011520761.1:p.Asn1280del
XM_011522460.1:c.3839_3841del	XP_011520762.1:p.Asn1280del
XM_011522461.1:c.*121_*123del	XP_011520763.1:n.*121_*123del
XM_011522458.3:c.3839_3841del	XP_011520760.1:p.Asn1280del
XM_011522461.3:c.*121_*123del	XP_011520763.1:n.*121_*123del
XM_017023172.1:c.4466_4468del	XP_016878661.1:p.Asn1489del
XM_017023173.1:c.*121_*123del	XP_016878662.1:n.*121_*123del
NM_001134407.3:c.4310_4312del MANE Select	NP_001127879.1:p.Asn1437del
NM_000833.5:c.4310_4312del	NP_000824.1:p.Asn1437del