Canonical Allele Identifier: CA2255437187
Gene: ADAP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30956218G= , CM000679.2:g.30956218G= GRCh38
NC_000017.10:g.29283236G= , CM000679.1:g.29283236G= GRCh37
NC_000017.9:g.26307362G= NCBI36
NG_051975.1:g.39483G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000330889.8:c.883-23G= MANE Select ENSP00000329468.3:n.883-23G=
ENST00000330889.7:c.883-23G= ENSP00000329468.3:n.883-23G=
ENST00000470962.1:n.303-23G=
ENST00000480980.1:n.317-23G=
ENST00000580525.5:c.901-23G= ENSP00000464121.1:n.901-23G=
ENST00000581285.5:c.799-23G= ENSP00000464155.1:n.799-23G=
ENST00000584828.5:c.252-23G=
ENST00000584989.1:c.175-23G= ENSP00000462634.1:n.175-23G=
ENST00000585130.5:c.*482-23G= ENSP00000464120.1:n.*482-23G=
NM_018404.2:c.883-23G= NP_060874.1:n.883-23G=
XM_005258008.2:c.901-23G= XP_005258065.1:n.901-23G=
XM_005258011.2:c.838-23G= XP_005258068.1:n.838-23G=
XM_006721973.2:c.901-23G= XP_006722036.1:n.901-23G=
XM_011524993.1:c.898-23G= XP_011523295.1:n.898-23G=
XM_011524994.1:c.880-23G= XP_011523296.1:n.880-23G=
NM_001346712.1:c.901-23G= NP_001333641.1:n.901-23G=
NM_001346714.1:c.880-23G= NP_001333643.1:n.880-23G=
NM_001346716.1:c.883-23G= NP_001333645.1:n.883-23G=
NR_144488.1:n.1082-23G=
XM_024450831.1:c.883-23G= XP_024306599.1:n.883-23G=
XM_024450832.1:c.898-23G= XP_024306600.1:n.898-23G=
XM_024450833.1:c.838-23G= XP_024306601.1:n.838-23G=
XM_024450834.1:c.901-23G= XP_024306602.1:n.901-23G=
XM_024450835.1:c.517-23G= XP_024306603.1:n.517-23G=
NM_018404.3:c.883-23G= MANE Select NP_060874.1:n.883-23G=
NM_001346712.2:c.901-23G= NP_001333641.1:n.901-23G=
NM_001346714.2:c.880-23G= NP_001333643.1:n.880-23G=
NM_001346716.2:c.883-23G= NP_001333645.1:n.883-23G=
NR_144488.2:n.873-23G=