Canonical Allele Identifier: CA1528441825
Gene: DNAH5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13793933T= , CM000667.2:g.13793933T= GRCh38
NC_000005.9:g.13794042T= , CM000667.1:g.13794042T= GRCh37
NC_000005.8:g.13847042T= NCBI36
NG_013081.1:g.155548A=
NG_013081.2:g.155548A=

Transcript Alleles

HGVS Amino-acid change
ENST00000265104.5:c.8010+3A= MANE Select ENSP00000265104.4:n.8010+3A=
ENST00000681290.1:c.7965+3A= ENSP00000505288.1:n.7965+3A=
ENST00000265104.4:c.8010+3A= ENSP00000265104.4:n.8010+3A=
NM_001369.2:c.8010+3A= NP_001360.1:n.8010+3A=
XM_005248262.2:c.7965+3A= XP_005248319.1:n.7965+3A=
XM_011513990.1:c.8010+3A= XP_011512292.1:n.8010+3A=
XR_925598.1:n.8217+3A=
XM_005248262.3:c.8118+3A= XP_005248319.2:n.8118+3A=
XM_017009177.1:c.8118+3A= XP_016864666.1:n.8118+3A=
XM_017009178.1:c.7023+3A= XP_016864667.1:n.7023+3A=
XM_017009179.2:c.7023+3A= XP_016864668.1:n.7023+3A=
XM_017009180.1:c.8118+3A= XP_016864669.1:n.8118+3A=
XM_017009181.1:c.8118+3A= XP_016864670.1:n.8118+3A=
XM_017009182.1:c.8118+3A= XP_016864671.1:n.8118+3A=
XM_017009183.1:c.8118+3A= XP_016864672.1:n.8118+3A=
XM_017009184.1:c.8118+3A= XP_016864673.1:n.8118+3A=
XM_017009185.1:c.3207+3A= XP_016864674.1:n.3207+3A=
XM_017009186.1:c.2760+3A= XP_016864675.1:n.2760+3A=
XM_017009188.1:c.2097+3A= XP_016864677.1:n.2097+3A=
XM_024454388.1:c.7023+3A= XP_024310156.1:n.7023+3A=
XM_024454389.1:c.6612+3A= XP_024310157.1:n.6612+3A=
XR_001742034.1:n.8135+3A=
XR_001742035.1:n.8135+3A=
NM_001369.3:c.8010+3A= MANE Select NP_001360.1:n.8010+3A=