Canonical Allele Identifier: CA2255437249

Gene: ADAP2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30956267T= , CM000679.2:g.30956267T=	GRCh38
NC_000017.10:g.29283285T= , CM000679.1:g.29283285T=	GRCh37
NC_000017.9:g.26307411T=	NCBI36
NG_051975.1:g.39532T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330889.8:c.909T= MANE Select	ENSP00000329468.3:p.Phe303=
ENST00000330889.7:c.909T=	ENSP00000329468.3:p.Phe303=
ENST00000470962.1:n.329T=
ENST00000480980.1:n.343T=
ENST00000580525.5:c.927T=	ENSP00000464121.1:p.Phe309=
ENST00000581285.5:c.825T=	ENSP00000464155.1:p.Phe275=
ENST00000584828.5:c.278T=
ENST00000584989.1:c.201T=	ENSP00000462634.1:p.Phe67=
ENST00000585130.5:c.*508T=	ENSP00000464120.1:n.*508T=
NM_018404.2:c.909T=	NP_060874.1:p.Phe303=
XM_005258008.2:c.927T=	XP_005258065.1:p.Phe309=
XM_005258011.2:c.864T=	XP_005258068.1:p.Phe288=
XM_006721973.2:c.927T=	XP_006722036.1:p.Phe309=
XM_011524993.1:c.924T=	XP_011523295.1:p.Phe308=
XM_011524994.1:c.906T=	XP_011523296.1:p.Phe302=
NM_001346712.1:c.927T=	NP_001333641.1:p.Phe309=
NM_001346714.1:c.906T=	NP_001333643.1:p.Phe302=
NM_001346716.1:c.909T=	NP_001333645.1:p.Phe303=
NR_144488.1:n.1108T=
XM_024450831.1:c.909T=	XP_024306599.1:p.Phe303=
XM_024450832.1:c.924T=	XP_024306600.1:p.Phe308=
XM_024450833.1:c.864T=	XP_024306601.1:p.Phe288=
XM_024450834.1:c.927T=	XP_024306602.1:p.Phe309=
XM_024450835.1:c.543T=	XP_024306603.1:p.Phe181=
NM_018404.3:c.909T= MANE Select	NP_060874.1:p.Phe303=
NM_001346712.2:c.927T=	NP_001333641.1:p.Phe309=
NM_001346714.2:c.906T=	NP_001333643.1:p.Phe302=
NM_001346716.2:c.909T=	NP_001333645.1:p.Phe303=
NR_144488.2:n.899T=