Canonical Allele Identifier: CA1528430583
Gene: DNAH5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13769472A= , CM000667.2:g.13769472A= GRCh38
NC_000005.9:g.13769581A= , CM000667.1:g.13769581A= GRCh37
NC_000005.8:g.13822581A= NCBI36
NG_013081.1:g.180009T=
NG_013081.2:g.180009T=

Transcript Alleles

HGVS Amino-acid change
ENST00000265104.5:c.9720+29T= MANE Select ENSP00000265104.4:n.9720+29T=
ENST00000681290.1:c.9675+29T= ENSP00000505288.1:n.9675+29T=
ENST00000265104.4:c.9720+29T= ENSP00000265104.4:n.9720+29T=
ENST00000504001.3:n.432+29T=
NM_001369.2:c.9720+29T= NP_001360.1:n.9720+29T=
XM_005248262.2:c.9675+29T= XP_005248319.1:n.9675+29T=
XM_005248262.3:c.9828+29T= XP_005248319.2:n.9828+29T=
XM_017009177.1:c.9828+29T= XP_016864666.1:n.9828+29T=
XM_017009178.1:c.8733+29T= XP_016864667.1:n.8733+29T=
XM_017009179.2:c.8733+29T= XP_016864668.1:n.8733+29T=
XM_017009180.1:c.9828+29T= XP_016864669.1:n.9828+29T=
XM_017009181.1:c.9828+29T= XP_016864670.1:n.9828+29T=
XM_017009182.1:c.9828+29T= XP_016864671.1:n.9828+29T=
XM_017009185.1:c.4917+29T= XP_016864674.1:n.4917+29T=
XM_017009186.1:c.4470+29T= XP_016864675.1:n.4470+29T=
XM_017009188.1:c.3807+29T= XP_016864677.1:n.3807+29T=
XM_024454388.1:c.8733+29T= XP_024310156.1:n.8733+29T=
XM_024454389.1:c.8322+29T= XP_024310157.1:n.8322+29T=
NM_001369.3:c.9720+29T= MANE Select NP_001360.1:n.9720+29T=