Canonical Allele Identifier: CA1528476192
Gene: DNAH5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13866202A= , CM000667.2:g.13866202A= GRCh38
NC_000005.9:g.13866311A= , CM000667.1:g.13866311A= GRCh37
NC_000005.8:g.13919311A= NCBI36
NG_013081.1:g.83279T=
NG_013081.2:g.83279T=

Transcript Alleles

HGVS Amino-acid change
ENST00000265104.5:c.4116+18T= MANE Select ENSP00000265104.4:n.4116+18T=
ENST00000681290.1:c.4071+18T= ENSP00000505288.1:n.4071+18T=
ENST00000265104.4:c.4116+18T= ENSP00000265104.4:n.4116+18T=
NM_001369.2:c.4116+18T= NP_001360.1:n.4116+18T=
XM_005248262.2:c.4071+18T= XP_005248319.1:n.4071+18T=
XM_011513990.1:c.4116+18T= XP_011512292.1:n.4116+18T=
XR_925598.1:n.4323+18T=
XM_005248262.3:c.4224+18T= XP_005248319.2:n.4224+18T=
XM_017009177.1:c.4224+18T= XP_016864666.1:n.4224+18T=
XM_017009178.1:c.3129+18T= XP_016864667.1:n.3129+18T=
XM_017009179.2:c.3129+18T= XP_016864668.1:n.3129+18T=
XM_017009180.1:c.4224+18T= XP_016864669.1:n.4224+18T=
XM_017009181.1:c.4224+18T= XP_016864670.1:n.4224+18T=
XM_017009182.1:c.4224+18T= XP_016864671.1:n.4224+18T=
XM_017009183.1:c.4224+18T= XP_016864672.1:n.4224+18T=
XM_017009184.1:c.4224+18T= XP_016864673.1:n.4224+18T=
XM_017009187.1:c.4224+18T= XP_016864676.1:n.4224+18T=
XM_024454388.1:c.3129+18T= XP_024310156.1:n.3129+18T=
XM_024454389.1:c.2718+18T= XP_024310157.1:n.2718+18T=
XR_001742034.1:n.4241+18T=
XR_001742035.1:n.4241+18T=
NM_001369.3:c.4116+18T= MANE Select NP_001360.1:n.4116+18T=