Canonical Allele Identifier: CA1528490480

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13901481G= , CM000667.2:g.13901481G=	GRCh38
NC_000005.9:g.13901590G= , CM000667.1:g.13901590G=	GRCh37
NC_000005.8:g.13954590G=	NCBI36
NG_013081.1:g.48000C=
NG_013081.2:g.48000C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.1823C= MANE Select	ENSP00000265104.4:p.Thr608=
ENST00000681290.1:c.1778C=	ENSP00000505288.1:p.Thr593=
ENST00000265104.4:c.1823C=	ENSP00000265104.4:p.Thr608=
NM_001369.2:c.1823C=	NP_001360.1:p.Thr608=
XM_005248262.2:c.1778C=	XP_005248319.1:p.Thr593=
XM_011513990.1:c.1823C=	XP_011512292.1:p.Thr608=
XR_925598.1:n.2030C=
XM_005248262.3:c.1931C=	XP_005248319.2:p.Thr644=
XM_017009177.1:c.1931C=	XP_016864666.1:p.Thr644=
XM_017009178.1:c.836C=	XP_016864667.1:p.Thr279=
XM_017009179.2:c.836C=	XP_016864668.1:p.Thr279=
XM_017009180.1:c.1931C=	XP_016864669.1:p.Thr644=
XM_017009181.1:c.1931C=	XP_016864670.1:p.Thr644=
XM_017009182.1:c.1931C=	XP_016864671.1:p.Thr644=
XM_017009183.1:c.1931C=	XP_016864672.1:p.Thr644=
XM_017009184.1:c.1931C=	XP_016864673.1:p.Thr644=
XM_017009187.1:c.1931C=	XP_016864676.1:p.Thr644=
XM_024454388.1:c.836C=	XP_024310156.1:p.Thr279=
XM_024454389.1:c.425C=	XP_024310157.1:p.Thr142=
XR_001742034.1:n.1948C=
XR_001742035.1:n.1948C=
NM_001369.3:c.1823C= MANE Select	NP_001360.1:p.Thr608=