Canonical Allele Identifier: CA398979674
Gene: ADAP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30956469A>T , CM000679.2:g.30956469A>T GRCh38
NC_000017.10:g.29283487A>T , CM000679.1:g.29283487A>T GRCh37
NC_000017.9:g.26307613A>T NCBI36
NG_051975.1:g.39734A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000330889.8:c.1111A>T MANE Select ENSP00000329468.3:p.Thr371Ser
ENST00000330889.7:c.1111A>T ENSP00000329468.3:p.Thr371Ser
ENST00000470962.1:n.531A>T
ENST00000480980.1:n.545A>T
ENST00000580525.5:c.1129A>T ENSP00000464121.1:p.Thr377Ser
ENST00000584828.5:c.402+78A>T
ENST00000585130.5:c.*710A>T ENSP00000464120.1:n.*710A>T
NM_018404.2:c.1111A>T NP_060874.1:p.Thr371Ser
XM_005258008.2:c.1129A>T XP_005258065.1:p.Thr377Ser
XM_005258011.2:c.1066A>T XP_005258068.1:p.Thr356Ser
XM_006721973.2:c.1051+78A>T XP_006722036.1:n.1051+78A>T
XM_011524993.1:c.1126A>T XP_011523295.1:p.Thr376Ser
XM_011524994.1:c.1108A>T XP_011523296.1:p.Thr370Ser
NM_001346712.1:c.1129A>T NP_001333641.1:p.Thr377Ser
NM_001346714.1:c.1108A>T NP_001333643.1:p.Thr370Ser
NM_001346716.1:c.1033+78A>T NP_001333645.1:n.1033+78A>T
NR_144488.1:n.1310A>T
XM_024450831.1:c.1111A>T XP_024306599.1:p.Ser371Cys
XM_024450832.1:c.1126A>T XP_024306600.1:p.Thr376Ser
XM_024450833.1:c.1066A>T XP_024306601.1:p.Thr356Ser
XM_024450834.1:c.1051+78A>T XP_024306602.1:n.1051+78A>T
XM_024450835.1:c.745A>T XP_024306603.1:p.Thr249Ser
NM_018404.3:c.1111A>T MANE Select NP_060874.1:p.Thr371Ser
NM_001346712.2:c.1129A>T NP_001333641.1:p.Thr377Ser
NM_001346714.2:c.1108A>T NP_001333643.1:p.Thr370Ser
NM_001346716.2:c.1033+78A>T NP_001333645.1:n.1033+78A>T
NR_144488.2:n.1101A>T