Canonical Allele Identifier: CA2255437136

Gene: ADAP2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30956172G= , CM000679.2:g.30956172G=	GRCh38
NC_000017.10:g.29283190G= , CM000679.1:g.29283190G=	GRCh37
NC_000017.9:g.26307316G=	NCBI36
NG_051975.1:g.39437G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330889.8:c.883-69G= MANE Select	ENSP00000329468.3:n.883-69G=
ENST00000330889.7:c.883-69G=	ENSP00000329468.3:n.883-69G=
ENST00000470962.1:n.303-69G=
ENST00000480980.1:n.317-69G=
ENST00000580525.5:c.901-69G=	ENSP00000464121.1:n.901-69G=
ENST00000581285.5:c.799-69G=	ENSP00000464155.1:n.799-69G=
ENST00000584828.5:c.252-69G=
ENST00000584989.1:c.175-69G=	ENSP00000462634.1:n.175-69G=
ENST00000585130.5:c.*482-69G=	ENSP00000464120.1:n.*482-69G=
NM_018404.2:c.883-69G=	NP_060874.1:n.883-69G=
XM_005258008.2:c.901-69G=	XP_005258065.1:n.901-69G=
XM_005258011.2:c.838-69G=	XP_005258068.1:n.838-69G=
XM_006721973.2:c.901-69G=	XP_006722036.1:n.901-69G=
XM_011524993.1:c.898-69G=	XP_011523295.1:n.898-69G=
XM_011524994.1:c.880-69G=	XP_011523296.1:n.880-69G=
NM_001346712.1:c.901-69G=	NP_001333641.1:n.901-69G=
NM_001346714.1:c.880-69G=	NP_001333643.1:n.880-69G=
NM_001346716.1:c.883-69G=	NP_001333645.1:n.883-69G=
NR_144488.1:n.1082-69G=
XM_024450831.1:c.883-69G=	XP_024306599.1:n.883-69G=
XM_024450832.1:c.898-69G=	XP_024306600.1:n.898-69G=
XM_024450833.1:c.838-69G=	XP_024306601.1:n.838-69G=
XM_024450834.1:c.901-69G=	XP_024306602.1:n.901-69G=
XM_024450835.1:c.517-69G=	XP_024306603.1:n.517-69G=
NM_018404.3:c.883-69G= MANE Select	NP_060874.1:n.883-69G=
NM_001346712.2:c.901-69G=	NP_001333641.1:n.901-69G=
NM_001346714.2:c.880-69G=	NP_001333643.1:n.880-69G=
NM_001346716.2:c.883-69G=	NP_001333645.1:n.883-69G=
NR_144488.2:n.873-69G=