Canonical Allele Identifier: CA1528490407

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13901320T= , CM000667.2:g.13901320T=	GRCh38
NC_000005.9:g.13901429T= , CM000667.1:g.13901429T=	GRCh37
NC_000005.8:g.13954429T=	NCBI36
NG_013081.1:g.48161A=
NG_013081.2:g.48161A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.1984A= MANE Select	ENSP00000265104.4:p.Ser662=
ENST00000681290.1:c.1939A=	ENSP00000505288.1:p.Ser647=
ENST00000265104.4:c.1984A=	ENSP00000265104.4:p.Ser662=
NM_001369.2:c.1984A=	NP_001360.1:p.Ser662=
XM_005248262.2:c.1939A=	XP_005248319.1:p.Ser647=
XM_011513990.1:c.1984A=	XP_011512292.1:p.Ser662=
XR_925598.1:n.2191A=
XM_005248262.3:c.2092A=	XP_005248319.2:p.Ser698=
XM_017009177.1:c.2092A=	XP_016864666.1:p.Ser698=
XM_017009178.1:c.997A=	XP_016864667.1:p.Ser333=
XM_017009179.2:c.997A=	XP_016864668.1:p.Ser333=
XM_017009180.1:c.2092A=	XP_016864669.1:p.Ser698=
XM_017009181.1:c.2092A=	XP_016864670.1:p.Ser698=
XM_017009182.1:c.2092A=	XP_016864671.1:p.Ser698=
XM_017009183.1:c.2092A=	XP_016864672.1:p.Ser698=
XM_017009184.1:c.2092A=	XP_016864673.1:p.Ser698=
XM_017009187.1:c.2092A=	XP_016864676.1:p.Ser698=
XM_024454388.1:c.997A=	XP_024310156.1:p.Ser333=
XM_024454389.1:c.586A=	XP_024310157.1:p.Ser196=
XR_001742034.1:n.2109A=
XR_001742035.1:n.2109A=
NM_001369.3:c.1984A= MANE Select	NP_001360.1:p.Ser662=