Canonical Allele Identifier: CA919824506

Gene: ADAP2

Linked Data

• dbSNP Id: rs1567728362

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30956273del , CM000679.2:g.30956273del	GRCh38
NC_000017.10:g.29283291del , CM000679.1:g.29283291del	GRCh37
NC_000017.9:g.26307417del	NCBI36
NG_051975.1:g.39538del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330889.8:c.915del MANE Select	ENSP00000329468.3:p.Asn306ThrfsTer?
ENST00000330889.7:c.915del	ENSP00000329468.3:p.Asn306ThrfsTer?
ENST00000470962.1:n.335del
ENST00000480980.1:n.349del
ENST00000580525.5:c.933del	ENSP00000464121.1:p.Asn312ThrfsTer?
ENST00000581285.5:c.831del	ENSP00000464155.1:p.Asn278ThrfsTer?
ENST00000584828.5:c.284del
ENST00000584989.1:c.207del	ENSP00000462634.1:p.Asn70ThrfsTer?
ENST00000585130.5:c.*514del	ENSP00000464120.1:n.*514del
NM_018404.2:c.915del	NP_060874.1:p.Asn306ThrfsTer?
XM_005258008.2:c.933del	XP_005258065.1:p.Asn312ThrfsTer?
XM_005258011.2:c.870del	XP_005258068.1:p.Asn291ThrfsTer?
XM_006721973.2:c.933del	XP_006722036.1:p.Asn312ThrfsTer?
XM_011524993.1:c.930del	XP_011523295.1:p.Asn311ThrfsTer?
XM_011524994.1:c.912del	XP_011523296.1:p.Asn305ThrfsTer?
NM_001346712.1:c.933del	NP_001333641.1:p.Asn312ThrfsTer?
NM_001346714.1:c.912del	NP_001333643.1:p.Asn305ThrfsTer?
NM_001346716.1:c.915del	NP_001333645.1:p.Asn306ThrfsTer?
NR_144488.1:n.1114del
XM_024450831.1:c.915del	XP_024306599.1:p.Asn306ThrfsTer?
XM_024450832.1:c.930del	XP_024306600.1:p.Asn311ThrfsTer?
XM_024450833.1:c.870del	XP_024306601.1:p.Asn291ThrfsTer?
XM_024450834.1:c.933del	XP_024306602.1:p.Asn312ThrfsTer?
XM_024450835.1:c.549del	XP_024306603.1:p.Asn184ThrfsTer?
NM_018404.3:c.915del MANE Select	NP_060874.1:p.Asn306ThrfsTer?
NM_001346712.2:c.933del	NP_001333641.1:p.Asn312ThrfsTer?
NM_001346714.2:c.912del	NP_001333643.1:p.Asn305ThrfsTer?
NM_001346716.2:c.915del	NP_001333645.1:p.Asn306ThrfsTer?
NR_144488.2:n.905del