Canonical Allele Identifier: CA2346496280

Gene: DNAAF9

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3271278A= , CM000682.2:g.3271278A=	GRCh38
NC_000020.10:g.3251924A= , CM000682.1:g.3251924A=	GRCh37
NC_000020.9:g.3199924A=	NCBI36
NG_031974.1:g.141386T=
NG_031974.2:g.141385T=

Transcript Alleles

HGVS	Amino-acid Change
NM_001009984.3:c.2651-716T= MANE Select	NP_001009984.1:n.2651-716T=
ENST00000252032.10:c.2651-716T= MANE Select	ENSP00000252032.9:n.2651-716T=
NM_001009984.2:c.2651-716T=	NP_001009984.1:n.2651-716T=
ENST00000252032.9:c.2651-716T=	ENSP00000252032.9:n.2651-716T=
XM_005260684.2:c.2648-716T=	XP_005260741.1:n.2648-716T=
XM_005260684.4:c.2648-716T=	XP_005260741.1:n.2648-716T=
XM_005260687.3:c.896-716T=	XP_005260744.1:n.896-716T=
XM_005260687.5:c.896-716T=	XP_005260744.1:n.896-716T=
XM_006723556.2:c.2573-716T=	XP_006723619.1:n.2573-716T=
XM_011529207.1:c.1673-716T=	XP_011527509.1:n.1673-716T=
XM_011529208.1:c.896-716T=	XP_011527510.1:n.896-716T=
XM_011529208.3:c.896-716T=	XP_011527510.1:n.896-716T=
XM_017027783.2:c.1673-716T=	XP_016883272.1:n.1673-716T=
XR_001754226.2:n.2665-716T=