Canonical Allele Identifier: CA1528476270
Gene: DNAH5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13870728T= , CM000667.2:g.13870728T= GRCh38
NC_000005.9:g.13870837T= , CM000667.1:g.13870837T= GRCh37
NC_000005.8:g.13923837T= NCBI36
NG_013081.1:g.78753A=
NG_013081.2:g.78753A=

Transcript Alleles

HGVS Amino-acid change
ENST00000265104.5:c.3834+39A= MANE Select ENSP00000265104.4:n.3834+39A=
ENST00000681290.1:c.3789+39A= ENSP00000505288.1:n.3789+39A=
ENST00000265104.4:c.3834+39A= ENSP00000265104.4:n.3834+39A=
NM_001369.2:c.3834+39A= NP_001360.1:n.3834+39A=
XM_005248262.2:c.3789+39A= XP_005248319.1:n.3789+39A=
XM_011513990.1:c.3834+39A= XP_011512292.1:n.3834+39A=
XR_925598.1:n.4041+39A=
XM_005248262.3:c.3942+39A= XP_005248319.2:n.3942+39A=
XM_017009177.1:c.3942+39A= XP_016864666.1:n.3942+39A=
XM_017009178.1:c.2847+39A= XP_016864667.1:n.2847+39A=
XM_017009179.2:c.2847+39A= XP_016864668.1:n.2847+39A=
XM_017009180.1:c.3942+39A= XP_016864669.1:n.3942+39A=
XM_017009181.1:c.3942+39A= XP_016864670.1:n.3942+39A=
XM_017009182.1:c.3942+39A= XP_016864671.1:n.3942+39A=
XM_017009183.1:c.3942+39A= XP_016864672.1:n.3942+39A=
XM_017009184.1:c.3942+39A= XP_016864673.1:n.3942+39A=
XM_017009187.1:c.3942+39A= XP_016864676.1:n.3942+39A=
XM_024454388.1:c.2847+39A= XP_024310156.1:n.2847+39A=
XM_024454389.1:c.2436+39A= XP_024310157.1:n.2436+39A=
XR_001742034.1:n.3959+39A=
XR_001742035.1:n.3959+39A=
NM_001369.3:c.3834+39A= MANE Select NP_001360.1:n.3834+39A=