Canonical Allele Identifier: CA2255437329

Gene: ADAP2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30956463C= , CM000679.2:g.30956463C=	GRCh38
NC_000017.10:g.29283481C= , CM000679.1:g.29283481C=	GRCh37
NC_000017.9:g.26307607C=	NCBI36
NG_051975.1:g.39728C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330889.8:c.1105C= MANE Select	ENSP00000329468.3:p.Arg369=
ENST00000330889.7:c.1105C=	ENSP00000329468.3:p.Arg369=
ENST00000470962.1:n.525C=
ENST00000480980.1:n.539C=
ENST00000580525.5:c.1123C=	ENSP00000464121.1:p.Arg375=
ENST00000584828.5:c.402+72C=
ENST00000585130.5:c.*704C=	ENSP00000464120.1:n.*704C=
NM_018404.2:c.1105C=	NP_060874.1:p.Arg369=
XM_005258008.2:c.1123C=	XP_005258065.1:p.Arg375=
XM_005258011.2:c.1060C=	XP_005258068.1:p.Arg354=
XM_006721973.2:c.1051+72C=	XP_006722036.1:n.1051+72C=
XM_011524993.1:c.1120C=	XP_011523295.1:p.Arg374=
XM_011524994.1:c.1102C=	XP_011523296.1:p.Arg368=
NM_001346712.1:c.1123C=	NP_001333641.1:p.Arg375=
NM_001346714.1:c.1102C=	NP_001333643.1:p.Arg368=
NM_001346716.1:c.1033+72C=	NP_001333645.1:n.1033+72C=
NR_144488.1:n.1304C=
XM_024450831.1:c.1105C=	XP_024306599.1:p.Arg369=
XM_024450832.1:c.1120C=	XP_024306600.1:p.Arg374=
XM_024450833.1:c.1060C=	XP_024306601.1:p.Arg354=
XM_024450834.1:c.1051+72C=	XP_024306602.1:n.1051+72C=
XM_024450835.1:c.739C=	XP_024306603.1:p.Arg247=
NM_018404.3:c.1105C= MANE Select	NP_060874.1:p.Arg369=
NM_001346712.2:c.1123C=	NP_001333641.1:p.Arg375=
NM_001346714.2:c.1102C=	NP_001333643.1:p.Arg368=
NM_001346716.2:c.1033+72C=	NP_001333645.1:n.1033+72C=
NR_144488.2:n.1095C=