Canonical Allele Identifier: CA1528422922
Gene: DNAH5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13752157T= , CM000667.2:g.13752157T= GRCh38
NC_000005.9:g.13752266T= , CM000667.1:g.13752266T= GRCh37
NC_000005.8:g.13805266T= NCBI36
NG_013081.1:g.197324A=
NG_013081.2:g.197324A=

Transcript Alleles

HGVS Amino-acid change
ENST00000265104.5:c.11005A= MANE Select ENSP00000265104.4:p.Ile3669=
ENST00000681290.1:c.10960A= ENSP00000505288.1:p.Ile3654=
ENST00000265104.4:c.11005A= ENSP00000265104.4:p.Ile3669=
NM_001369.2:c.11005A= NP_001360.1:p.Ile3669=
XM_005248262.2:c.10960A= XP_005248319.1:p.Ile3654=
XM_005248262.3:c.11113A= XP_005248319.2:p.Ile3705=
XM_017009177.1:c.11113A= XP_016864666.1:p.Ile3705=
XM_017009178.1:c.10018A= XP_016864667.1:p.Ile3340=
XM_017009179.2:c.10018A= XP_016864668.1:p.Ile3340=
XM_017009180.1:c.11113A= XP_016864669.1:p.Ile3705=
XM_017009181.1:c.11113A= XP_016864670.1:p.Ile3705=
XM_017009182.1:c.11113A= XP_016864671.1:p.Ile3705=
XM_017009185.1:c.6202A= XP_016864674.1:p.Ile2068=
XM_017009186.1:c.5755A= XP_016864675.1:p.Ile1919=
XM_017009188.1:c.5092A= XP_016864677.1:p.Ile1698=
XM_024454388.1:c.10018A= XP_024310156.1:p.Ile3340=
XM_024454389.1:c.9607A= XP_024310157.1:p.Ile3203=
NM_001369.3:c.11005A= MANE Select NP_001360.1:p.Ile3669=