Canonical Allele Identifier: CA398979389
Gene: ADAP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30956391A>T , CM000679.2:g.30956391A>T GRCh38
NC_000017.10:g.29283409A>T , CM000679.1:g.29283409A>T GRCh37
NC_000017.9:g.26307535A>T NCBI36
NG_051975.1:g.39656A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000330889.8:c.1033A>T MANE Select ENSP00000329468.3:p.Ser345Cys
ENST00000330889.7:c.1033A>T ENSP00000329468.3:p.Ser345Cys
ENST00000470962.1:n.453A>T
ENST00000480980.1:n.467A>T
ENST00000580525.5:c.1051A>T ENSP00000464121.1:p.Ser351Cys
ENST00000581285.5:c.949A>T ENSP00000464155.1:p.Ser317Cys
ENST00000584828.5:c.402A>T
ENST00000585130.5:c.*632A>T ENSP00000464120.1:n.*632A>T
NM_018404.2:c.1033A>T NP_060874.1:p.Ser345Cys
XM_005258008.2:c.1051A>T XP_005258065.1:p.Ser351Cys
XM_005258011.2:c.988A>T XP_005258068.1:p.Ser330Cys
XM_006721973.2:c.1051A>T XP_006722036.1:p.Thr351Ser
XM_011524993.1:c.1048A>T XP_011523295.1:p.Ser350Cys
XM_011524994.1:c.1030A>T XP_011523296.1:p.Ser344Cys
NM_001346712.1:c.1051A>T NP_001333641.1:p.Ser351Cys
NM_001346714.1:c.1030A>T NP_001333643.1:p.Ser344Cys
NM_001346716.1:c.1033A>T NP_001333645.1:p.Thr345Ser
NR_144488.1:n.1232A>T
XM_024450831.1:c.1033A>T XP_024306599.1:p.Ser345Cys
XM_024450832.1:c.1048A>T XP_024306600.1:p.Ser350Cys
XM_024450833.1:c.988A>T XP_024306601.1:p.Ser330Cys
XM_024450834.1:c.1051A>T XP_024306602.1:p.Thr351Ser
XM_024450835.1:c.667A>T XP_024306603.1:p.Ser223Cys
NM_018404.3:c.1033A>T MANE Select NP_060874.1:p.Ser345Cys
NM_001346712.2:c.1051A>T NP_001333641.1:p.Ser351Cys
NM_001346714.2:c.1030A>T NP_001333643.1:p.Ser344Cys
NM_001346716.2:c.1033A>T NP_001333645.1:p.Thr345Ser
NR_144488.2:n.1023A>T