Canonical Allele Identifier: CA1528458757
Gene: DNAH5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13830640A= , CM000667.2:g.13830640A= GRCh38
NC_000005.9:g.13830749A= , CM000667.1:g.13830749A= GRCh37
NC_000005.8:g.13883749A= NCBI36
NG_013081.1:g.118841T=
NG_013081.2:g.118841T=

Transcript Alleles

HGVS Amino-acid change
ENST00000683090.1:n.949T=
ENST00000265104.5:c.6018T= MANE Select ENSP00000265104.4:p.Cys2006=
ENST00000681290.1:c.5973T= ENSP00000505288.1:p.Cys1991=
ENST00000265104.4:c.6018T= ENSP00000265104.4:p.Cys2006=
NM_001369.2:c.6018T= NP_001360.1:p.Cys2006=
XM_005248262.2:c.5973T= XP_005248319.1:p.Cys1991=
XM_011513990.1:c.6018T= XP_011512292.1:p.Cys2006=
XR_925598.1:n.6225T=
XM_005248262.3:c.6126T= XP_005248319.2:p.Cys2042=
XM_017009177.1:c.6126T= XP_016864666.1:p.Cys2042=
XM_017009178.1:c.5031T= XP_016864667.1:p.Cys1677=
XM_017009179.2:c.5031T= XP_016864668.1:p.Cys1677=
XM_017009180.1:c.6126T= XP_016864669.1:p.Cys2042=
XM_017009181.1:c.6126T= XP_016864670.1:p.Cys2042=
XM_017009182.1:c.6126T= XP_016864671.1:p.Cys2042=
XM_017009183.1:c.6126T= XP_016864672.1:p.Cys2042=
XM_017009184.1:c.6126T= XP_016864673.1:p.Cys2042=
XM_017009185.1:c.1215T= XP_016864674.1:p.Cys405=
XM_017009186.1:c.768T= XP_016864675.1:p.Cys256=
XM_017009187.1:c.6126T= XP_016864676.1:p.Cys2042=
XM_017009188.1:c.105T= XP_016864677.1:p.Cys35=
XM_024454388.1:c.5031T= XP_024310156.1:p.Cys1677=
XM_024454389.1:c.4620T= XP_024310157.1:p.Cys1540=
XR_001742034.1:n.6143T=
XR_001742035.1:n.6143T=
NM_001369.3:c.6018T= MANE Select NP_001360.1:p.Cys2006=