Canonical Allele Identifier: CA359217070

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13850729A>T , CM000667.2:g.13850729A>T	GRCh38
NC_000005.9:g.13850838A>T , CM000667.1:g.13850838A>T	GRCh37
NC_000005.8:g.13903838A>T	NCBI36
NG_013081.1:g.98752T>A
NG_013081.2:g.98752T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001369.3:c.5037T>A MANE Select	NP_001360.1:p.Cys1679Ter
ENST00000265104.5:c.5037T>A MANE Select	ENSP00000265104.4:p.Cys1679Ter
NM_001369.2:c.5037T>A	NP_001360.1:p.Cys1679Ter
ENST00000265104.4:c.5037T>A	ENSP00000265104.4:p.Cys1679Ter
ENST00000681290.1:c.4992T>A	ENSP00000505288.1:p.Cys1664Ter
XM_005248262.2:c.4992T>A	XP_005248319.1:p.Cys1664Ter
XM_005248262.3:c.5145T>A	XP_005248319.2:p.Cys1715Ter
XM_011513990.1:c.5037T>A	XP_011512292.1:p.Cys1679Ter
XM_017009177.1:c.5145T>A	XP_016864666.1:p.Cys1715Ter
XM_017009178.1:c.4050T>A	XP_016864667.1:p.Cys1350Ter
XM_017009179.2:c.4050T>A	XP_016864668.1:p.Cys1350Ter
XM_017009180.1:c.5145T>A	XP_016864669.1:p.Cys1715Ter
XM_017009181.1:c.5145T>A	XP_016864670.1:p.Cys1715Ter
XM_017009182.1:c.5145T>A	XP_016864671.1:p.Cys1715Ter
XM_017009183.1:c.5145T>A	XP_016864672.1:p.Cys1715Ter
XM_017009184.1:c.5145T>A	XP_016864673.1:p.Cys1715Ter
XM_017009185.1:c.234T>A	XP_016864674.1:p.Cys78Ter
XM_017009186.1:c.-57T>A	XP_016864675.1:n.-57T>A
XM_017009187.1:c.5145T>A	XP_016864676.1:p.Cys1715Ter
XM_024454388.1:c.4050T>A	XP_024310156.1:p.Cys1350Ter
XM_024454389.1:c.3639T>A	XP_024310157.1:p.Cys1213Ter
XR_001742034.1:n.5162T>A
XR_001742035.1:n.5162T>A
XR_925598.1:n.5244T>A