Canonical Allele Identifier: CA1528476470
Gene: DNAH5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13870930T= , CM000667.2:g.13870930T= GRCh38
NC_000005.9:g.13871039T= , CM000667.1:g.13871039T= GRCh37
NC_000005.8:g.13924039T= NCBI36
NG_013081.1:g.78551A=
NG_013081.2:g.78551A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000265104.5:c.3671A= MANE Select ENSP00000265104.4:p.Lys1224=
ENST00000681290.1:c.3626A= ENSP00000505288.1:p.Lys1209=
ENST00000265104.4:c.3671A= ENSP00000265104.4:p.Lys1224=
NM_001369.2:c.3671A= NP_001360.1:p.Lys1224=
XM_005248262.2:c.3626A= XP_005248319.1:p.Lys1209=
XM_011513990.1:c.3671A= XP_011512292.1:p.Lys1224=
XR_925598.1:n.3878A=
XM_005248262.3:c.3779A= XP_005248319.2:p.Lys1260=
XM_017009177.1:c.3779A= XP_016864666.1:p.Lys1260=
XM_017009178.1:c.2684A= XP_016864667.1:p.Lys895=
XM_017009179.2:c.2684A= XP_016864668.1:p.Lys895=
XM_017009180.1:c.3779A= XP_016864669.1:p.Lys1260=
XM_017009181.1:c.3779A= XP_016864670.1:p.Lys1260=
XM_017009182.1:c.3779A= XP_016864671.1:p.Lys1260=
XM_017009183.1:c.3779A= XP_016864672.1:p.Lys1260=
XM_017009184.1:c.3779A= XP_016864673.1:p.Lys1260=
XM_017009187.1:c.3779A= XP_016864676.1:p.Lys1260=
XM_024454388.1:c.2684A= XP_024310156.1:p.Lys895=
XM_024454389.1:c.2273A= XP_024310157.1:p.Lys758=
XR_001742034.1:n.3796A=
XR_001742035.1:n.3796A=
NM_001369.3:c.3671A= MANE Select NP_001360.1:p.Lys1224=