Canonical Allele Identifier: CA2255437306
Gene: ADAP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30956401A= , CM000679.2:g.30956401A= GRCh38
NC_000017.10:g.29283419A= , CM000679.1:g.29283419A= GRCh37
NC_000017.9:g.26307545A= NCBI36
NG_051975.1:g.39666A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000330889.8:c.1043A= MANE Select ENSP00000329468.3:p.Glu348=
ENST00000330889.7:c.1043A= ENSP00000329468.3:p.Glu348=
ENST00000470962.1:n.463A=
ENST00000480980.1:n.477A=
ENST00000580525.5:c.1061A= ENSP00000464121.1:p.Glu354=
ENST00000581285.5:c.959A= ENSP00000464155.1:p.Glu320=
ENST00000584828.5:c.402+10A=
ENST00000585130.5:c.*642A= ENSP00000464120.1:n.*642A=
NM_018404.2:c.1043A= NP_060874.1:p.Glu348=
XM_005258008.2:c.1061A= XP_005258065.1:p.Glu354=
XM_005258011.2:c.998A= XP_005258068.1:p.Glu333=
XM_006721973.2:c.1051+10A= XP_006722036.1:n.1051+10A=
XM_011524993.1:c.1058A= XP_011523295.1:p.Glu353=
XM_011524994.1:c.1040A= XP_011523296.1:p.Glu347=
NM_001346712.1:c.1061A= NP_001333641.1:p.Glu354=
NM_001346714.1:c.1040A= NP_001333643.1:p.Glu347=
NM_001346716.1:c.1033+10A= NP_001333645.1:n.1033+10A=
NR_144488.1:n.1242A=
XM_024450831.1:c.1043A= XP_024306599.1:p.Glu348=
XM_024450832.1:c.1058A= XP_024306600.1:p.Glu353=
XM_024450833.1:c.998A= XP_024306601.1:p.Glu333=
XM_024450834.1:c.1051+10A= XP_024306602.1:n.1051+10A=
XM_024450835.1:c.677A= XP_024306603.1:p.Glu226=
NM_018404.3:c.1043A= MANE Select NP_060874.1:p.Glu348=
NM_001346712.2:c.1061A= NP_001333641.1:p.Glu354=
NM_001346714.2:c.1040A= NP_001333643.1:p.Glu347=
NM_001346716.2:c.1033+10A= NP_001333645.1:n.1033+10A=
NR_144488.2:n.1033A=