Canonical Allele Identifier: CA1528403773
Gene: DNAH5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13708238C= , CM000667.2:g.13708238C= GRCh38
NC_000005.9:g.13708347C= , CM000667.1:g.13708347C= GRCh37
NC_000005.8:g.13761347C= NCBI36
NG_013081.1:g.241243G=
NG_013081.2:g.241243G=

Transcript Alleles

HGVS Amino-acid change
ENST00000683611.1:n.556G=
ENST00000265104.5:c.13223G= MANE Select ENSP00000265104.4:p.Arg4408=
ENST00000681290.1:c.13178G= ENSP00000505288.1:p.Arg4393=
ENST00000265104.4:c.13223G= ENSP00000265104.4:p.Arg4408=
NM_001369.2:c.13223G= NP_001360.1:p.Arg4408=
XM_005248262.2:c.13178G= XP_005248319.1:p.Arg4393=
XM_005248262.3:c.13331G= XP_005248319.2:p.Arg4444=
XM_017009177.1:c.12911G= XP_016864666.1:p.Arg4304=
XM_017009178.1:c.12236G= XP_016864667.1:p.Arg4079=
XM_017009179.2:c.12236G= XP_016864668.1:p.Arg4079=
XM_017009185.1:c.8420G= XP_016864674.1:p.Arg2807=
XM_017009186.1:c.7973G= XP_016864675.1:p.Arg2658=
XM_017009188.1:c.7310G= XP_016864677.1:p.Arg2437=
XM_024454388.1:c.12236G= XP_024310156.1:p.Arg4079=
XM_024454389.1:c.11825G= XP_024310157.1:p.Arg3942=
NM_001369.3:c.13223G= MANE Select NP_001360.1:p.Arg4408=