Canonical Allele Identifier: CA2255437311

Gene: ADAP2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30956427C= , CM000679.2:g.30956427C=	GRCh38
NC_000017.10:g.29283445C= , CM000679.1:g.29283445C=	GRCh37
NC_000017.9:g.26307571C=	NCBI36
NG_051975.1:g.39692C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330889.8:c.1069C= MANE Select	ENSP00000329468.3:p.Arg357=
ENST00000330889.7:c.1069C=	ENSP00000329468.3:p.Arg357=
ENST00000470962.1:n.489C=
ENST00000480980.1:n.503C=
ENST00000580525.5:c.1087C=	ENSP00000464121.1:p.Arg363=
ENST00000581285.5:c.985C=	ENSP00000464155.1:p.Arg329=
ENST00000584828.5:c.402+36C=
ENST00000585130.5:c.*668C=	ENSP00000464120.1:n.*668C=
NM_018404.2:c.1069C=	NP_060874.1:p.Arg357=
XM_005258008.2:c.1087C=	XP_005258065.1:p.Arg363=
XM_005258011.2:c.1024C=	XP_005258068.1:p.Arg342=
XM_006721973.2:c.1051+36C=	XP_006722036.1:n.1051+36C=
XM_011524993.1:c.1084C=	XP_011523295.1:p.Arg362=
XM_011524994.1:c.1066C=	XP_011523296.1:p.Arg356=
NM_001346712.1:c.1087C=	NP_001333641.1:p.Arg363=
NM_001346714.1:c.1066C=	NP_001333643.1:p.Arg356=
NM_001346716.1:c.1033+36C=	NP_001333645.1:n.1033+36C=
NR_144488.1:n.1268C=
XM_024450831.1:c.1069C=	XP_024306599.1:p.Arg357=
XM_024450832.1:c.1084C=	XP_024306600.1:p.Arg362=
XM_024450833.1:c.1024C=	XP_024306601.1:p.Arg342=
XM_024450834.1:c.1051+36C=	XP_024306602.1:n.1051+36C=
XM_024450835.1:c.703C=	XP_024306603.1:p.Arg235=
NM_018404.3:c.1069C= MANE Select	NP_060874.1:p.Arg357=
NM_001346712.2:c.1087C=	NP_001333641.1:p.Arg363=
NM_001346714.2:c.1066C=	NP_001333643.1:p.Arg356=
NM_001346716.2:c.1033+36C=	NP_001333645.1:n.1033+36C=
NR_144488.2:n.1059C=