Canonical Allele Identifier: CA2255437255

Gene: ADAP2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30956276C= , CM000679.2:g.30956276C=	GRCh38
NC_000017.10:g.29283294C= , CM000679.1:g.29283294C=	GRCh37
NC_000017.9:g.26307420C=	NCBI36
NG_051975.1:g.39541C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330889.8:c.918C= MANE Select	ENSP00000329468.3:p.Asn306=
ENST00000330889.7:c.918C=	ENSP00000329468.3:p.Asn306=
ENST00000470962.1:n.338C=
ENST00000480980.1:n.352C=
ENST00000580525.5:c.936C=	ENSP00000464121.1:p.Asn312=
ENST00000581285.5:c.834C=	ENSP00000464155.1:p.Asn278=
ENST00000584828.5:c.287C=
ENST00000584989.1:c.210C=	ENSP00000462634.1:p.Asn70=
ENST00000585130.5:c.*517C=	ENSP00000464120.1:n.*517C=
NM_018404.2:c.918C=	NP_060874.1:p.Asn306=
XM_005258008.2:c.936C=	XP_005258065.1:p.Asn312=
XM_005258011.2:c.873C=	XP_005258068.1:p.Asn291=
XM_006721973.2:c.936C=	XP_006722036.1:p.Asn312=
XM_011524993.1:c.933C=	XP_011523295.1:p.Asn311=
XM_011524994.1:c.915C=	XP_011523296.1:p.Asn305=
NM_001346712.1:c.936C=	NP_001333641.1:p.Asn312=
NM_001346714.1:c.915C=	NP_001333643.1:p.Asn305=
NM_001346716.1:c.918C=	NP_001333645.1:p.Asn306=
NR_144488.1:n.1117C=
XM_024450831.1:c.918C=	XP_024306599.1:p.Asn306=
XM_024450832.1:c.933C=	XP_024306600.1:p.Asn311=
XM_024450833.1:c.873C=	XP_024306601.1:p.Asn291=
XM_024450834.1:c.936C=	XP_024306602.1:p.Asn312=
XM_024450835.1:c.552C=	XP_024306603.1:p.Asn184=
NM_018404.3:c.918C= MANE Select	NP_060874.1:p.Asn306=
NM_001346712.2:c.936C=	NP_001333641.1:p.Asn312=
NM_001346714.2:c.915C=	NP_001333643.1:p.Asn305=
NM_001346716.2:c.918C=	NP_001333645.1:p.Asn306=
NR_144488.2:n.908C=