Canonical Allele Identifier: CA398979568
Gene: ADAP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30956442A>C , CM000679.2:g.30956442A>C GRCh38
NC_000017.10:g.29283460A>C , CM000679.1:g.29283460A>C GRCh37
NC_000017.9:g.26307586A>C NCBI36
NG_051975.1:g.39707A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000330889.8:c.1084A>C MANE Select ENSP00000329468.3:p.Ser362Arg
ENST00000330889.7:c.1084A>C ENSP00000329468.3:p.Ser362Arg
ENST00000470962.1:n.504A>C
ENST00000480980.1:n.518A>C
ENST00000580525.5:c.1102A>C ENSP00000464121.1:p.Ser368Arg
ENST00000581285.5:c.1000A>C
ENST00000584828.5:c.402+51A>C
ENST00000585130.5:c.*683A>C ENSP00000464120.1:n.*683A>C
NM_018404.2:c.1084A>C NP_060874.1:p.Ser362Arg
XM_005258008.2:c.1102A>C XP_005258065.1:p.Ser368Arg
XM_005258011.2:c.1039A>C XP_005258068.1:p.Ser347Arg
XM_006721973.2:c.1051+51A>C XP_006722036.1:n.1051+51A>C
XM_011524993.1:c.1099A>C XP_011523295.1:p.Ser367Arg
XM_011524994.1:c.1081A>C XP_011523296.1:p.Ser361Arg
NM_001346712.1:c.1102A>C NP_001333641.1:p.Ser368Arg
NM_001346714.1:c.1081A>C NP_001333643.1:p.Ser361Arg
NM_001346716.1:c.1033+51A>C NP_001333645.1:n.1033+51A>C
NR_144488.1:n.1283A>C
XM_024450831.1:c.1084A>C XP_024306599.1:p.Ser362Arg
XM_024450832.1:c.1099A>C XP_024306600.1:p.Ser367Arg
XM_024450833.1:c.1039A>C XP_024306601.1:p.Ser347Arg
XM_024450834.1:c.1051+51A>C XP_024306602.1:n.1051+51A>C
XM_024450835.1:c.718A>C XP_024306603.1:p.Ser240Arg
NM_018404.3:c.1084A>C MANE Select NP_060874.1:p.Ser362Arg
NM_001346712.2:c.1102A>C NP_001333641.1:p.Ser368Arg
NM_001346714.2:c.1081A>C NP_001333643.1:p.Ser361Arg
NM_001346716.2:c.1033+51A>C NP_001333645.1:n.1033+51A>C
NR_144488.2:n.1074A>C