Canonical Allele Identifier: CA2255437250

Gene: ADAP2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30956268C= , CM000679.2:g.30956268C=	GRCh38
NC_000017.10:g.29283286C= , CM000679.1:g.29283286C=	GRCh37
NC_000017.9:g.26307412C=	NCBI36
NG_051975.1:g.39533C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330889.8:c.910C= MANE Select	ENSP00000329468.3:p.Leu304=
ENST00000330889.7:c.910C=	ENSP00000329468.3:p.Leu304=
ENST00000470962.1:n.330C=
ENST00000480980.1:n.344C=
ENST00000580525.5:c.928C=	ENSP00000464121.1:p.Leu310=
ENST00000581285.5:c.826C=	ENSP00000464155.1:p.Leu276=
ENST00000584828.5:c.279C=
ENST00000584989.1:c.202C=	ENSP00000462634.1:p.Leu68=
ENST00000585130.5:c.*509C=	ENSP00000464120.1:n.*509C=
NM_018404.2:c.910C=	NP_060874.1:p.Leu304=
XM_005258008.2:c.928C=	XP_005258065.1:p.Leu310=
XM_005258011.2:c.865C=	XP_005258068.1:p.Leu289=
XM_006721973.2:c.928C=	XP_006722036.1:p.Leu310=
XM_011524993.1:c.925C=	XP_011523295.1:p.Leu309=
XM_011524994.1:c.907C=	XP_011523296.1:p.Leu303=
NM_001346712.1:c.928C=	NP_001333641.1:p.Leu310=
NM_001346714.1:c.907C=	NP_001333643.1:p.Leu303=
NM_001346716.1:c.910C=	NP_001333645.1:p.Leu304=
NR_144488.1:n.1109C=
XM_024450831.1:c.910C=	XP_024306599.1:p.Leu304=
XM_024450832.1:c.925C=	XP_024306600.1:p.Leu309=
XM_024450833.1:c.865C=	XP_024306601.1:p.Leu289=
XM_024450834.1:c.928C=	XP_024306602.1:p.Leu310=
XM_024450835.1:c.544C=	XP_024306603.1:p.Leu182=
NM_018404.3:c.910C= MANE Select	NP_060874.1:p.Leu304=
NM_001346712.2:c.928C=	NP_001333641.1:p.Leu310=
NM_001346714.2:c.907C=	NP_001333643.1:p.Leu303=
NM_001346716.2:c.910C=	NP_001333645.1:p.Leu304=
NR_144488.2:n.900C=