Canonical Allele Identifier: CA1528428259
Gene: DNAH5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13764310G= , CM000667.2:g.13764310G= GRCh38
NC_000005.9:g.13764419G= , CM000667.1:g.13764419G= GRCh37
NC_000005.8:g.13817419G= NCBI36
NG_013081.1:g.185171C=
NG_013081.2:g.185171C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000265104.5:c.10102-1409C= MANE Select ENSP00000265104.4:n.10102-1409C=
ENST00000681290.1:c.10057-1409C= ENSP00000505288.1:n.10057-1409C=
ENST00000265104.4:c.10102-1409C= ENSP00000265104.4:n.10102-1409C=
ENST00000504001.3:n.610-1409C=
NM_001369.2:c.10102-1409C= NP_001360.1:n.10102-1409C=
XM_005248262.2:c.10057-1409C= XP_005248319.1:n.10057-1409C=
XM_005248262.3:c.10210-1409C= XP_005248319.2:n.10210-1409C=
XM_017009177.1:c.10210-1409C= XP_016864666.1:n.10210-1409C=
XM_017009178.1:c.9115-1409C= XP_016864667.1:n.9115-1409C=
XM_017009179.2:c.9115-1409C= XP_016864668.1:n.9115-1409C=
XM_017009180.1:c.10210-1409C= XP_016864669.1:n.10210-1409C=
XM_017009181.1:c.10210-1409C= XP_016864670.1:n.10210-1409C=
XM_017009182.1:c.10210-1409C= XP_016864671.1:n.10210-1409C=
XM_017009185.1:c.5299-1409C= XP_016864674.1:n.5299-1409C=
XM_017009186.1:c.4852-1409C= XP_016864675.1:n.4852-1409C=
XM_017009188.1:c.4189-1409C= XP_016864677.1:n.4189-1409C=
XM_024454388.1:c.9115-1409C= XP_024310156.1:n.9115-1409C=
XM_024454389.1:c.8704-1409C= XP_024310157.1:n.8704-1409C=
NM_001369.3:c.10102-1409C= MANE Select NP_001360.1:n.10102-1409C=