Canonical Allele Identifier: CA398979573
Gene: ADAP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30956443G>T , CM000679.2:g.30956443G>T GRCh38
NC_000017.10:g.29283461G>T , CM000679.1:g.29283461G>T GRCh37
NC_000017.9:g.26307587G>T NCBI36
NG_051975.1:g.39708G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000330889.8:c.1085G>T MANE Select ENSP00000329468.3:p.Ser362Ile
ENST00000330889.7:c.1085G>T ENSP00000329468.3:p.Ser362Ile
ENST00000470962.1:n.505G>T
ENST00000480980.1:n.519G>T
ENST00000580525.5:c.1103G>T ENSP00000464121.1:p.Ser368Ile
ENST00000584828.5:c.402+52G>T
ENST00000585130.5:c.*684G>T ENSP00000464120.1:n.*684G>T
NM_018404.2:c.1085G>T NP_060874.1:p.Ser362Ile
XM_005258008.2:c.1103G>T XP_005258065.1:p.Ser368Ile
XM_005258011.2:c.1040G>T XP_005258068.1:p.Ser347Ile
XM_006721973.2:c.1051+52G>T XP_006722036.1:n.1051+52G>T
XM_011524993.1:c.1100G>T XP_011523295.1:p.Ser367Ile
XM_011524994.1:c.1082G>T XP_011523296.1:p.Ser361Ile
NM_001346712.1:c.1103G>T NP_001333641.1:p.Ser368Ile
NM_001346714.1:c.1082G>T NP_001333643.1:p.Ser361Ile
NM_001346716.1:c.1033+52G>T NP_001333645.1:n.1033+52G>T
NR_144488.1:n.1284G>T
XM_024450831.1:c.1085G>T XP_024306599.1:p.Ser362Ile
XM_024450832.1:c.1100G>T XP_024306600.1:p.Ser367Ile
XM_024450833.1:c.1040G>T XP_024306601.1:p.Ser347Ile
XM_024450834.1:c.1051+52G>T XP_024306602.1:n.1051+52G>T
XM_024450835.1:c.719G>T XP_024306603.1:p.Ser240Ile
NM_018404.3:c.1085G>T MANE Select NP_060874.1:p.Ser362Ile
NM_001346712.2:c.1103G>T NP_001333641.1:p.Ser368Ile
NM_001346714.2:c.1082G>T NP_001333643.1:p.Ser361Ile
NM_001346716.2:c.1033+52G>T NP_001333645.1:n.1033+52G>T
NR_144488.2:n.1075G>T