Canonical Allele Identifier: CA2255437243

Gene: ADAP2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30956250G= , CM000679.2:g.30956250G=	GRCh38
NC_000017.10:g.29283268G= , CM000679.1:g.29283268G=	GRCh37
NC_000017.9:g.26307394G=	NCBI36
NG_051975.1:g.39515G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330889.8:c.892G= MANE Select	ENSP00000329468.3:p.Glu298=
ENST00000330889.7:c.892G=	ENSP00000329468.3:p.Glu298=
ENST00000470962.1:n.312G=
ENST00000480980.1:n.326G=
ENST00000580525.5:c.910G=	ENSP00000464121.1:p.Glu304=
ENST00000581285.5:c.808G=	ENSP00000464155.1:p.Glu270=
ENST00000584828.5:c.261G=
ENST00000584989.1:c.184G=	ENSP00000462634.1:p.Glu62=
ENST00000585130.5:c.*491G=	ENSP00000464120.1:n.*491G=
NM_018404.2:c.892G=	NP_060874.1:p.Glu298=
XM_005258008.2:c.910G=	XP_005258065.1:p.Glu304=
XM_005258011.2:c.847G=	XP_005258068.1:p.Glu283=
XM_006721973.2:c.910G=	XP_006722036.1:p.Glu304=
XM_011524993.1:c.907G=	XP_011523295.1:p.Glu303=
XM_011524994.1:c.889G=	XP_011523296.1:p.Glu297=
NM_001346712.1:c.910G=	NP_001333641.1:p.Glu304=
NM_001346714.1:c.889G=	NP_001333643.1:p.Glu297=
NM_001346716.1:c.892G=	NP_001333645.1:p.Glu298=
NR_144488.1:n.1091G=
XM_024450831.1:c.892G=	XP_024306599.1:p.Glu298=
XM_024450832.1:c.907G=	XP_024306600.1:p.Glu303=
XM_024450833.1:c.847G=	XP_024306601.1:p.Glu283=
XM_024450834.1:c.910G=	XP_024306602.1:p.Glu304=
XM_024450835.1:c.526G=	XP_024306603.1:p.Glu176=
NM_018404.3:c.892G= MANE Select	NP_060874.1:p.Glu298=
NM_001346712.2:c.910G=	NP_001333641.1:p.Glu304=
NM_001346714.2:c.889G=	NP_001333643.1:p.Glu297=
NM_001346716.2:c.892G=	NP_001333645.1:p.Glu298=
NR_144488.2:n.882G=