Canonical Allele Identifier: CA2255437293

Gene: ADAP2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30956376G= , CM000679.2:g.30956376G=	GRCh38
NC_000017.10:g.29283394G= , CM000679.1:g.29283394G=	GRCh37
NC_000017.9:g.26307520G=	NCBI36
NG_051975.1:g.39641G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330889.8:c.1018G= MANE Select	ENSP00000329468.3:p.Val340=
ENST00000330889.7:c.1018G=	ENSP00000329468.3:p.Val340=
ENST00000470962.1:n.438G=
ENST00000480980.1:n.452G=
ENST00000580525.5:c.1036G=	ENSP00000464121.1:p.Val346=
ENST00000581285.5:c.934G=	ENSP00000464155.1:p.Val312=
ENST00000584828.5:c.387G=
ENST00000585130.5:c.*617G=	ENSP00000464120.1:n.*617G=
NM_018404.2:c.1018G=	NP_060874.1:p.Val340=
XM_005258008.2:c.1036G=	XP_005258065.1:p.Val346=
XM_005258011.2:c.973G=	XP_005258068.1:p.Val325=
XM_006721973.2:c.1036G=	XP_006722036.1:p.Val346=
XM_011524993.1:c.1033G=	XP_011523295.1:p.Val345=
XM_011524994.1:c.1015G=	XP_011523296.1:p.Val339=
NM_001346712.1:c.1036G=	NP_001333641.1:p.Val346=
NM_001346714.1:c.1015G=	NP_001333643.1:p.Val339=
NM_001346716.1:c.1018G=	NP_001333645.1:p.Val340=
NR_144488.1:n.1217G=
XM_024450831.1:c.1018G=	XP_024306599.1:p.Val340=
XM_024450832.1:c.1033G=	XP_024306600.1:p.Val345=
XM_024450833.1:c.973G=	XP_024306601.1:p.Val325=
XM_024450834.1:c.1036G=	XP_024306602.1:p.Val346=
XM_024450835.1:c.652G=	XP_024306603.1:p.Val218=
NM_018404.3:c.1018G= MANE Select	NP_060874.1:p.Val340=
NM_001346712.2:c.1036G=	NP_001333641.1:p.Val346=
NM_001346714.2:c.1015G=	NP_001333643.1:p.Val339=
NM_001346716.2:c.1018G=	NP_001333645.1:p.Val340=
NR_144488.2:n.1008G=