Canonical Allele Identifier: CA398979367
Gene: ADAP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30956386G>A , CM000679.2:g.30956386G>A GRCh38
NC_000017.10:g.29283404G>A , CM000679.1:g.29283404G>A GRCh37
NC_000017.9:g.26307530G>A NCBI36
NG_051975.1:g.39651G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000330889.8:c.1028G>A MANE Select ENSP00000329468.3:p.Cys343Tyr
ENST00000330889.7:c.1028G>A ENSP00000329468.3:p.Cys343Tyr
ENST00000470962.1:n.448G>A
ENST00000480980.1:n.462G>A
ENST00000580525.5:c.1046G>A ENSP00000464121.1:p.Cys349Tyr
ENST00000581285.5:c.944G>A ENSP00000464155.1:p.Cys315Tyr
ENST00000584828.5:c.397G>A
ENST00000585130.5:c.*627G>A ENSP00000464120.1:n.*627G>A
NM_018404.2:c.1028G>A NP_060874.1:p.Cys343Tyr
XM_005258008.2:c.1046G>A XP_005258065.1:p.Cys349Tyr
XM_005258011.2:c.983G>A XP_005258068.1:p.Cys328Tyr
XM_006721973.2:c.1046G>A XP_006722036.1:p.Cys349Tyr
XM_011524993.1:c.1043G>A XP_011523295.1:p.Cys348Tyr
XM_011524994.1:c.1025G>A XP_011523296.1:p.Cys342Tyr
NM_001346712.1:c.1046G>A NP_001333641.1:p.Cys349Tyr
NM_001346714.1:c.1025G>A NP_001333643.1:p.Cys342Tyr
NM_001346716.1:c.1028G>A NP_001333645.1:p.Cys343Tyr
NR_144488.1:n.1227G>A
XM_024450831.1:c.1028G>A XP_024306599.1:p.Cys343Tyr
XM_024450832.1:c.1043G>A XP_024306600.1:p.Cys348Tyr
XM_024450833.1:c.983G>A XP_024306601.1:p.Cys328Tyr
XM_024450834.1:c.1046G>A XP_024306602.1:p.Cys349Tyr
XM_024450835.1:c.662G>A XP_024306603.1:p.Cys221Tyr
NM_018404.3:c.1028G>A MANE Select NP_060874.1:p.Cys343Tyr
NM_001346712.2:c.1046G>A NP_001333641.1:p.Cys349Tyr
NM_001346714.2:c.1025G>A NP_001333643.1:p.Cys342Tyr
NM_001346716.2:c.1028G>A NP_001333645.1:p.Cys343Tyr
NR_144488.2:n.1018G>A