Canonical Allele Identifier: CA499227340
Gene: ADAP2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.29283459C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30956441C>A , CM000679.2:g.30956441C>A GRCh38
NC_000017.10:g.29283459C>A , CM000679.1:g.29283459C>A GRCh37
NC_000017.9:g.26307585C>A NCBI36
NG_051975.1:g.39706C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000330889.8:c.1083C>A MANE Select ENSP00000329468.3:p.Ser361=
ENST00000330889.7:c.1083C>A ENSP00000329468.3:p.Ser361=
ENST00000470962.1:n.503C>A
ENST00000480980.1:n.517C>A
ENST00000580525.5:c.1101C>A ENSP00000464121.1:p.Ser367=
ENST00000581285.5:c.999C>A ENSP00000464155.1:p.Ser333=
ENST00000584828.5:c.402+50C>A
ENST00000585130.5:c.*682C>A ENSP00000464120.1:n.*682C>A
NM_018404.2:c.1083C>A NP_060874.1:p.Ser361=
XM_005258008.2:c.1101C>A XP_005258065.1:p.Ser367=
XM_005258011.2:c.1038C>A XP_005258068.1:p.Ser346=
XM_006721973.2:c.1051+50C>A XP_006722036.1:n.1051+50C>A
XM_011524993.1:c.1098C>A XP_011523295.1:p.Ser366=
XM_011524994.1:c.1080C>A XP_011523296.1:p.Ser360=
NM_001346712.1:c.1101C>A NP_001333641.1:p.Ser367=
NM_001346714.1:c.1080C>A NP_001333643.1:p.Ser360=
NM_001346716.1:c.1033+50C>A NP_001333645.1:n.1033+50C>A
NR_144488.1:n.1282C>A
XM_024450831.1:c.1083C>A XP_024306599.1:p.Ser361=
XM_024450832.1:c.1098C>A XP_024306600.1:p.Ser366=
XM_024450833.1:c.1038C>A XP_024306601.1:p.Ser346=
XM_024450834.1:c.1051+50C>A XP_024306602.1:n.1051+50C>A
XM_024450835.1:c.717C>A XP_024306603.1:p.Ser239=
NM_018404.3:c.1083C>A MANE Select NP_060874.1:p.Ser361=
NM_001346712.2:c.1101C>A NP_001333641.1:p.Ser367=
NM_001346714.2:c.1080C>A NP_001333643.1:p.Ser360=
NM_001346716.2:c.1033+50C>A NP_001333645.1:n.1033+50C>A
NR_144488.2:n.1073C>A