Canonical Allele Identifier: CA2255437251

Gene: ADAP2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30956269T= , CM000679.2:g.30956269T=	GRCh38
NC_000017.10:g.29283287T= , CM000679.1:g.29283287T=	GRCh37
NC_000017.9:g.26307413T=	NCBI36
NG_051975.1:g.39534T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330889.8:c.911T= MANE Select	ENSP00000329468.3:p.Leu304=
ENST00000330889.7:c.911T=	ENSP00000329468.3:p.Leu304=
ENST00000470962.1:n.331T=
ENST00000480980.1:n.345T=
ENST00000580525.5:c.929T=	ENSP00000464121.1:p.Leu310=
ENST00000581285.5:c.827T=	ENSP00000464155.1:p.Leu276=
ENST00000584828.5:c.280T=
ENST00000584989.1:c.203T=	ENSP00000462634.1:p.Leu68=
ENST00000585130.5:c.*510T=	ENSP00000464120.1:n.*510T=
NM_018404.2:c.911T=	NP_060874.1:p.Leu304=
XM_005258008.2:c.929T=	XP_005258065.1:p.Leu310=
XM_005258011.2:c.866T=	XP_005258068.1:p.Leu289=
XM_006721973.2:c.929T=	XP_006722036.1:p.Leu310=
XM_011524993.1:c.926T=	XP_011523295.1:p.Leu309=
XM_011524994.1:c.908T=	XP_011523296.1:p.Leu303=
NM_001346712.1:c.929T=	NP_001333641.1:p.Leu310=
NM_001346714.1:c.908T=	NP_001333643.1:p.Leu303=
NM_001346716.1:c.911T=	NP_001333645.1:p.Leu304=
NR_144488.1:n.1110T=
XM_024450831.1:c.911T=	XP_024306599.1:p.Leu304=
XM_024450832.1:c.926T=	XP_024306600.1:p.Leu309=
XM_024450833.1:c.866T=	XP_024306601.1:p.Leu289=
XM_024450834.1:c.929T=	XP_024306602.1:p.Leu310=
XM_024450835.1:c.545T=	XP_024306603.1:p.Leu182=
NM_018404.3:c.911T= MANE Select	NP_060874.1:p.Leu304=
NM_001346712.2:c.929T=	NP_001333641.1:p.Leu310=
NM_001346714.2:c.908T=	NP_001333643.1:p.Leu303=
NM_001346716.2:c.911T=	NP_001333645.1:p.Leu304=
NR_144488.2:n.901T=