Canonical Allele Identifier: CA1528483781

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13885952C= , CM000667.2:g.13885952C=	GRCh38
NC_000005.9:g.13886061C= , CM000667.1:g.13886061C=	GRCh37
NC_000005.8:g.13939061C=	NCBI36
NG_013081.1:g.63529G=
NG_013081.2:g.63529G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.2743+12G= MANE Select	ENSP00000265104.4:n.2743+12G=
ENST00000681290.1:c.2698+12G=	ENSP00000505288.1:n.2698+12G=
ENST00000265104.4:c.2743+12G=	ENSP00000265104.4:n.2743+12G=
NM_001369.2:c.2743+12G=	NP_001360.1:n.2743+12G=
XM_005248262.2:c.2698+12G=	XP_005248319.1:n.2698+12G=
XM_011513990.1:c.2743+12G=	XP_011512292.1:n.2743+12G=
XR_925598.1:n.2950+12G=
XM_005248262.3:c.2851+12G=	XP_005248319.2:n.2851+12G=
XM_017009177.1:c.2851+12G=	XP_016864666.1:n.2851+12G=
XM_017009178.1:c.1756+12G=	XP_016864667.1:n.1756+12G=
XM_017009179.2:c.1756+12G=	XP_016864668.1:n.1756+12G=
XM_017009180.1:c.2851+12G=	XP_016864669.1:n.2851+12G=
XM_017009181.1:c.2851+12G=	XP_016864670.1:n.2851+12G=
XM_017009182.1:c.2851+12G=	XP_016864671.1:n.2851+12G=
XM_017009183.1:c.2851+12G=	XP_016864672.1:n.2851+12G=
XM_017009184.1:c.2851+12G=	XP_016864673.1:n.2851+12G=
XM_017009187.1:c.2851+12G=	XP_016864676.1:n.2851+12G=
XM_024454388.1:c.1756+12G=	XP_024310156.1:n.1756+12G=
XM_024454389.1:c.1345+12G=	XP_024310157.1:n.1345+12G=
XR_001742034.1:n.2868+12G=
XR_001742035.1:n.2868+12G=
NM_001369.3:c.2743+12G= MANE Select	NP_001360.1:n.2743+12G=