Canonical Allele Identifier: CA1528483818
Gene: DNAH5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13886036C= , CM000667.2:g.13886036C= GRCh38
NC_000005.9:g.13886145C= , CM000667.1:g.13886145C= GRCh37
NC_000005.8:g.13939145C= NCBI36
NG_013081.1:g.63445G=
NG_013081.2:g.63445G=

Transcript Alleles

HGVS Amino-acid change
ENST00000265104.5:c.2671G= MANE Select ENSP00000265104.4:p.Glu891=
ENST00000681290.1:c.2626G= ENSP00000505288.1:p.Glu876=
ENST00000265104.4:c.2671G= ENSP00000265104.4:p.Glu891=
NM_001369.2:c.2671G= NP_001360.1:p.Glu891=
XM_005248262.2:c.2626G= XP_005248319.1:p.Glu876=
XM_011513990.1:c.2671G= XP_011512292.1:p.Glu891=
XR_925598.1:n.2878G=
XM_005248262.3:c.2779G= XP_005248319.2:p.Glu927=
XM_017009177.1:c.2779G= XP_016864666.1:p.Glu927=
XM_017009178.1:c.1684G= XP_016864667.1:p.Glu562=
XM_017009179.2:c.1684G= XP_016864668.1:p.Glu562=
XM_017009180.1:c.2779G= XP_016864669.1:p.Glu927=
XM_017009181.1:c.2779G= XP_016864670.1:p.Glu927=
XM_017009182.1:c.2779G= XP_016864671.1:p.Glu927=
XM_017009183.1:c.2779G= XP_016864672.1:p.Glu927=
XM_017009184.1:c.2779G= XP_016864673.1:p.Glu927=
XM_017009187.1:c.2779G= XP_016864676.1:p.Glu927=
XM_024454388.1:c.1684G= XP_024310156.1:p.Glu562=
XM_024454389.1:c.1273G= XP_024310157.1:p.Glu425=
XR_001742034.1:n.2796G=
XR_001742035.1:n.2796G=
NM_001369.3:c.2671G= MANE Select NP_001360.1:p.Glu891=