Canonical Allele Identifier: CA8485034
Gene: ADAP2 HGNC NCBI

Linked Data

dbSNP Id: rs769470362

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30956222del , CM000679.2:g.30956222del GRCh38
NC_000017.10:g.29283240del , CM000679.1:g.29283240del GRCh37
NC_000017.9:g.26307366del NCBI36
NG_051975.1:g.39487del

Transcript Alleles

HGVS Amino-acid Change
ENST00000330889.8:c.883-19del MANE Select ENSP00000329468.3:n.883-19del
ENST00000330889.7:c.883-19del ENSP00000329468.3:n.883-19del
ENST00000470962.1:n.303-19del
ENST00000480980.1:n.317-19del
ENST00000580525.5:c.901-19del ENSP00000464121.1:n.901-19del
ENST00000581285.5:c.799-19del ENSP00000464155.1:n.799-19del
ENST00000584828.5:c.252-19del
ENST00000584989.1:c.175-19del ENSP00000462634.1:n.175-19del
ENST00000585130.5:c.*482-19del ENSP00000464120.1:n.*482-19del
NM_018404.2:c.883-19del NP_060874.1:n.883-19del
XM_005258008.2:c.901-19del XP_005258065.1:n.901-19del
XM_005258011.2:c.838-19del XP_005258068.1:n.838-19del
XM_006721973.2:c.901-19del XP_006722036.1:n.901-19del
XM_011524993.1:c.898-19del XP_011523295.1:n.898-19del
XM_011524994.1:c.880-19del XP_011523296.1:n.880-19del
NM_001346712.1:c.901-19del NP_001333641.1:n.901-19del
NM_001346714.1:c.880-19del NP_001333643.1:n.880-19del
NM_001346716.1:c.883-19del NP_001333645.1:n.883-19del
NR_144488.1:n.1082-19del
XM_024450831.1:c.883-19del XP_024306599.1:n.883-19del
XM_024450832.1:c.898-19del XP_024306600.1:n.898-19del
XM_024450833.1:c.838-19del XP_024306601.1:n.838-19del
XM_024450834.1:c.901-19del XP_024306602.1:n.901-19del
XM_024450835.1:c.517-19del XP_024306603.1:n.517-19del
NM_018404.3:c.883-19del MANE Select NP_060874.1:n.883-19del
NM_001346712.2:c.901-19del NP_001333641.1:n.901-19del
NM_001346714.2:c.880-19del NP_001333643.1:n.880-19del
NM_001346716.2:c.883-19del NP_001333645.1:n.883-19del
NR_144488.2:n.873-19del