Canonical Allele Identifier: CA2255437433
Gene: ADAP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30956671_30956672delinsCT , CM000679.2:g.30956671_30956672delinsCT GRCh38
NC_000017.10:g.29283689_29283690delinsCT , CM000679.1:g.29283689_29283690delinsCT GRCh37
NC_000017.9:g.26307815_26307816delinsCT NCBI36
NG_051975.1:g.39936_39937delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000330889.8:c.1111+202_1111+203delinsCT MANE Select ENSP00000329468.3:n.1111+202_1111+203delinsCT
ENST00000330889.7:c.1111+202_1111+203delinsCT ENSP00000329468.3:n.1111+202_1111+203delinsCT
ENST00000470962.1:n.531+202_531+203delinsCT
ENST00000480980.1:n.747_748delinsCT
ENST00000580525.5:c.1129+202_1129+203delinsCT ENSP00000464121.1:n.1129+202_1129+203delinsCT
ENST00000584828.5:c.402+280_402+281delinsCT
ENST00000585130.5:c.*710+202_*710+203delinsCT ENSP00000464120.1:n.*710+202_*710+203delinsCT
NM_018404.2:c.1111+202_1111+203delinsCT NP_060874.1:n.1111+202_1111+203delinsCT
XM_005258008.2:c.1129+202_1129+203delinsCT XP_005258065.1:n.1129+202_1129+203delinsCT
XM_005258011.2:c.1066+202_1066+203delinsCT XP_005258068.1:n.1066+202_1066+203delinsCT
XM_006721973.2:c.1051+280_1051+281delinsCT XP_006722036.1:n.1051+280_1051+281delinsCT
XM_011524993.1:c.1126+202_1126+203delinsCT XP_011523295.1:n.1126+202_1126+203delinsCT
XM_011524994.1:c.1108+202_1108+203delinsCT XP_011523296.1:n.1108+202_1108+203delinsCT
NM_001346712.1:c.1129+202_1129+203delinsCT NP_001333641.1:n.1129+202_1129+203delinsCT
NM_001346714.1:c.1108+202_1108+203delinsCT NP_001333643.1:n.1108+202_1108+203delinsCT
NM_001346716.1:c.1033+280_1033+281delinsCT NP_001333645.1:n.1033+280_1033+281delinsCT
NR_144488.1:n.1310+202_1310+203delinsCT
XM_024450832.1:c.1126+202_1126+203delinsCT XP_024306600.1:n.1126+202_1126+203delinsCT
XM_024450833.1:c.1066+202_1066+203delinsCT XP_024306601.1:n.1066+202_1066+203delinsCT
XM_024450834.1:c.1051+280_1051+281delinsCT XP_024306602.1:n.1051+280_1051+281delinsCT
XM_024450835.1:c.745+202_745+203delinsCT XP_024306603.1:n.745+202_745+203delinsCT
NM_018404.3:c.1111+202_1111+203delinsCT MANE Select NP_060874.1:n.1111+202_1111+203delinsCT
NM_001346712.2:c.1129+202_1129+203delinsCT NP_001333641.1:n.1129+202_1129+203delinsCT
NM_001346714.2:c.1108+202_1108+203delinsCT NP_001333643.1:n.1108+202_1108+203delinsCT
NM_001346716.2:c.1033+280_1033+281delinsCT NP_001333645.1:n.1033+280_1033+281delinsCT
NR_144488.2:n.1101+202_1101+203delinsCT