Canonical Allele Identifier: CA359222765

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13862748C>A , CM000667.2:g.13862748C>A	GRCh38
NC_000005.9:g.13862857C>A , CM000667.1:g.13862857C>A	GRCh37
NC_000005.8:g.13915857C>A	NCBI36
NG_013081.1:g.86733G>T
NG_013081.2:g.86733G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001369.3:c.4597-1G>T MANE Select	NP_001360.1:n.4597-1G>T
ENST00000265104.5:c.4597-1G>T MANE Select	ENSP00000265104.4:n.4597-1G>T
NM_001369.2:c.4597-1G>T	NP_001360.1:n.4597-1G>T
ENST00000265104.4:c.4597-1G>T	ENSP00000265104.4:n.4597-1G>T
ENST00000681290.1:c.4552-1G>T	ENSP00000505288.1:n.4552-1G>T
XM_005248262.2:c.4552-1G>T	XP_005248319.1:n.4552-1G>T
XM_005248262.3:c.4705-1G>T	XP_005248319.2:n.4705-1G>T
XM_011513990.1:c.4597-1G>T	XP_011512292.1:n.4597-1G>T
XM_017009177.1:c.4705-1G>T	XP_016864666.1:n.4705-1G>T
XM_017009178.1:c.3610-1G>T	XP_016864667.1:n.3610-1G>T
XM_017009179.2:c.3610-1G>T	XP_016864668.1:n.3610-1G>T
XM_017009180.1:c.4705-1G>T	XP_016864669.1:n.4705-1G>T
XM_017009181.1:c.4705-1G>T	XP_016864670.1:n.4705-1G>T
XM_017009182.1:c.4705-1G>T	XP_016864671.1:n.4705-1G>T
XM_017009183.1:c.4705-1G>T	XP_016864672.1:n.4705-1G>T
XM_017009184.1:c.4705-1G>T	XP_016864673.1:n.4705-1G>T
XM_017009187.1:c.4705-1G>T	XP_016864676.1:n.4705-1G>T
XM_024454388.1:c.3610-1G>T	XP_024310156.1:n.3610-1G>T
XM_024454389.1:c.3199-1G>T	XP_024310157.1:n.3199-1G>T
XR_001742034.1:n.4722-1G>T
XR_001742035.1:n.4722-1G>T
XR_925598.1:n.4804-1G>T