Canonical Allele Identifier: CA2255437295
Gene: ADAP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30956379C= , CM000679.2:g.30956379C= GRCh38
NC_000017.10:g.29283397C= , CM000679.1:g.29283397C= GRCh37
NC_000017.9:g.26307523C= NCBI36
NG_051975.1:g.39644C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000330889.8:c.1021C= MANE Select ENSP00000329468.3:p.Leu341=
ENST00000330889.7:c.1021C= ENSP00000329468.3:p.Leu341=
ENST00000470962.1:n.441C=
ENST00000480980.1:n.455C=
ENST00000580525.5:c.1039C= ENSP00000464121.1:p.Leu347=
ENST00000581285.5:c.937C= ENSP00000464155.1:p.Leu313=
ENST00000584828.5:c.390C=
ENST00000585130.5:c.*620C= ENSP00000464120.1:n.*620C=
NM_018404.2:c.1021C= NP_060874.1:p.Leu341=
XM_005258008.2:c.1039C= XP_005258065.1:p.Leu347=
XM_005258011.2:c.976C= XP_005258068.1:p.Leu326=
XM_006721973.2:c.1039C= XP_006722036.1:p.Leu347=
XM_011524993.1:c.1036C= XP_011523295.1:p.Leu346=
XM_011524994.1:c.1018C= XP_011523296.1:p.Leu340=
NM_001346712.1:c.1039C= NP_001333641.1:p.Leu347=
NM_001346714.1:c.1018C= NP_001333643.1:p.Leu340=
NM_001346716.1:c.1021C= NP_001333645.1:p.Leu341=
NR_144488.1:n.1220C=
XM_024450831.1:c.1021C= XP_024306599.1:p.Leu341=
XM_024450832.1:c.1036C= XP_024306600.1:p.Leu346=
XM_024450833.1:c.976C= XP_024306601.1:p.Leu326=
XM_024450834.1:c.1039C= XP_024306602.1:p.Leu347=
XM_024450835.1:c.655C= XP_024306603.1:p.Leu219=
NM_018404.3:c.1021C= MANE Select NP_060874.1:p.Leu341=
NM_001346712.2:c.1039C= NP_001333641.1:p.Leu347=
NM_001346714.2:c.1018C= NP_001333643.1:p.Leu340=
NM_001346716.2:c.1021C= NP_001333645.1:p.Leu341=
NR_144488.2:n.1011C=