Canonical Allele Identifier: CA398979589
Gene: ADAP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30956446C>T , CM000679.2:g.30956446C>T GRCh38
NC_000017.10:g.29283464C>T , CM000679.1:g.29283464C>T GRCh37
NC_000017.9:g.26307590C>T NCBI36
NG_051975.1:g.39711C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000330889.8:c.1088C>T MANE Select ENSP00000329468.3:p.Pro363Leu
ENST00000330889.7:c.1088C>T ENSP00000329468.3:p.Pro363Leu
ENST00000470962.1:n.508C>T
ENST00000480980.1:n.522C>T
ENST00000580525.5:c.1106C>T ENSP00000464121.1:p.Pro369Leu
ENST00000584828.5:c.402+55C>T
ENST00000585130.5:c.*687C>T ENSP00000464120.1:n.*687C>T
NM_018404.2:c.1088C>T NP_060874.1:p.Pro363Leu
XM_005258008.2:c.1106C>T XP_005258065.1:p.Pro369Leu
XM_005258011.2:c.1043C>T XP_005258068.1:p.Pro348Leu
XM_006721973.2:c.1051+55C>T XP_006722036.1:n.1051+55C>T
XM_011524993.1:c.1103C>T XP_011523295.1:p.Pro368Leu
XM_011524994.1:c.1085C>T XP_011523296.1:p.Pro362Leu
NM_001346712.1:c.1106C>T NP_001333641.1:p.Pro369Leu
NM_001346714.1:c.1085C>T NP_001333643.1:p.Pro362Leu
NM_001346716.1:c.1033+55C>T NP_001333645.1:n.1033+55C>T
NR_144488.1:n.1287C>T
XM_024450831.1:c.1088C>T XP_024306599.1:p.Pro363Leu
XM_024450832.1:c.1103C>T XP_024306600.1:p.Pro368Leu
XM_024450833.1:c.1043C>T XP_024306601.1:p.Pro348Leu
XM_024450834.1:c.1051+55C>T XP_024306602.1:n.1051+55C>T
XM_024450835.1:c.722C>T XP_024306603.1:p.Pro241Leu
NM_018404.3:c.1088C>T MANE Select NP_060874.1:p.Pro363Leu
NM_001346712.2:c.1106C>T NP_001333641.1:p.Pro369Leu
NM_001346714.2:c.1085C>T NP_001333643.1:p.Pro362Leu
NM_001346716.2:c.1033+55C>T NP_001333645.1:n.1033+55C>T
NR_144488.2:n.1078C>T