Canonical Allele Identifier: CA2277047812

Gene: DNAH17

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78567034C= , CM000679.2:g.78567034C=	GRCh38
NC_000017.10:g.76563116C= , CM000679.1:g.76563116C=	GRCh37
NC_000017.9:g.74074711C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389840.7:c.1417G= MANE Select	ENSP00000374490.6:p.Asp473=
ENST00000389840.6:c.1417G=	ENSP00000374490.6:p.Asp473=
ENST00000585328.5:c.1417G=	ENSP00000465516.1:p.Asp473=
ENST00000589793.1:n.629G=
NM_173628.3:c.1417G=	NP_775899.3:p.Asp473=
XM_011525416.1:c.1417G=	XP_011523718.1:p.Asp473=
XM_011525417.1:c.1417G=	XP_011523719.1:p.Asp473=
XR_934583.1:n.1578G=
XM_011525416.2:c.1417G=	XP_011523718.1:p.Asp473=
XM_024451013.1:c.1417G=	XP_024306781.1:p.Asp473=
XM_024451014.1:c.1417G=	XP_024306782.1:p.Asp473=
XR_002958080.1:n.1580G=
XR_002958081.1:n.1584G=
NM_173628.4:c.1417G= MANE Select	NP_775899.3:p.Asp473=