Canonical Allele Identifier: CA1528441612

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13793498A= , CM000667.2:g.13793498A=	GRCh38
NC_000005.9:g.13793607A= , CM000667.1:g.13793607A=	GRCh37
NC_000005.8:g.13846607A=	NCBI36
NG_013081.1:g.155983T=
NG_013081.2:g.155983T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.8224+17T= MANE Select	ENSP00000265104.4:n.8224+17T=
ENST00000681290.1:c.8179+17T=	ENSP00000505288.1:n.8179+17T=
ENST00000265104.4:c.8224+17T=	ENSP00000265104.4:n.8224+17T=
NM_001369.2:c.8224+17T=	NP_001360.1:n.8224+17T=
XM_005248262.2:c.8179+17T=	XP_005248319.1:n.8179+17T=
XM_011513990.1:c.8224+17T=	XP_011512292.1:n.8224+17T=
XR_925598.1:n.8431+17T=
XM_005248262.3:c.8332+17T=	XP_005248319.2:n.8332+17T=
XM_017009177.1:c.8332+17T=	XP_016864666.1:n.8332+17T=
XM_017009178.1:c.7237+17T=	XP_016864667.1:n.7237+17T=
XM_017009179.2:c.7237+17T=	XP_016864668.1:n.7237+17T=
XM_017009180.1:c.8332+17T=	XP_016864669.1:n.8332+17T=
XM_017009181.1:c.8332+17T=	XP_016864670.1:n.8332+17T=
XM_017009182.1:c.8332+17T=	XP_016864671.1:n.8332+17T=
XM_017009183.1:c.8332+17T=	XP_016864672.1:n.8332+17T=
XM_017009184.1:c.8332+17T=	XP_016864673.1:n.8332+17T=
XM_017009185.1:c.3421+17T=	XP_016864674.1:n.3421+17T=
XM_017009186.1:c.2974+17T=	XP_016864675.1:n.2974+17T=
XM_017009188.1:c.2311+17T=	XP_016864677.1:n.2311+17T=
XM_024454388.1:c.7237+17T=	XP_024310156.1:n.7237+17T=
XM_024454389.1:c.6826+17T=	XP_024310157.1:n.6826+17T=
XR_001742034.1:n.8349+17T=
XR_001742035.1:n.8349+17T=
NM_001369.3:c.8224+17T= MANE Select	NP_001360.1:n.8224+17T=