Canonical Allele Identifier: CA2255437388

Gene: ADAP2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30956591A= , CM000679.2:g.30956591A=	GRCh38
NC_000017.10:g.29283609A= , CM000679.1:g.29283609A=	GRCh37
NC_000017.9:g.26307735A=	NCBI36
NG_051975.1:g.39856A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330889.8:c.1111+122A= MANE Select	ENSP00000329468.3:n.1111+122A=
ENST00000330889.7:c.1111+122A=	ENSP00000329468.3:n.1111+122A=
ENST00000470962.1:n.531+122A=
ENST00000480980.1:n.667A=
ENST00000580525.5:c.1129+122A=	ENSP00000464121.1:n.1129+122A=
ENST00000584828.5:c.402+200A=
ENST00000585130.5:c.*710+122A=	ENSP00000464120.1:n.*710+122A=
NM_018404.2:c.1111+122A=	NP_060874.1:n.1111+122A=
XM_005258008.2:c.1129+122A=	XP_005258065.1:n.1129+122A=
XM_005258011.2:c.1066+122A=	XP_005258068.1:n.1066+122A=
XM_006721973.2:c.1051+200A=	XP_006722036.1:n.1051+200A=
XM_011524993.1:c.1126+122A=	XP_011523295.1:n.1126+122A=
XM_011524994.1:c.1108+122A=	XP_011523296.1:n.1108+122A=
NM_001346712.1:c.1129+122A=	NP_001333641.1:n.1129+122A=
NM_001346714.1:c.1108+122A=	NP_001333643.1:n.1108+122A=
NM_001346716.1:c.1033+200A=	NP_001333645.1:n.1033+200A=
NR_144488.1:n.1310+122A=
XM_024450831.1:c.*21A=	XP_024306599.1:n.*21A=
XM_024450832.1:c.1126+122A=	XP_024306600.1:n.1126+122A=
XM_024450833.1:c.1066+122A=	XP_024306601.1:n.1066+122A=
XM_024450834.1:c.1051+200A=	XP_024306602.1:n.1051+200A=
XM_024450835.1:c.745+122A=	XP_024306603.1:n.745+122A=
NM_018404.3:c.1111+122A= MANE Select	NP_060874.1:n.1111+122A=
NM_001346712.2:c.1129+122A=	NP_001333641.1:n.1129+122A=
NM_001346714.2:c.1108+122A=	NP_001333643.1:n.1108+122A=
NM_001346716.2:c.1033+200A=	NP_001333645.1:n.1033+200A=
NR_144488.2:n.1101+122A=