Canonical Allele Identifier: CA1528423527
Gene: DNAH5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13753478A= , CM000667.2:g.13753478A= GRCh38
NC_000005.9:g.13753587A= , CM000667.1:g.13753587A= GRCh37
NC_000005.8:g.13806587A= NCBI36
NG_013081.1:g.196003T=
NG_013081.2:g.196003T=

Transcript Alleles

HGVS Amino-acid change
ENST00000265104.5:c.10627T= MANE Select ENSP00000265104.4:p.Leu3543=
ENST00000681290.1:c.10582T= ENSP00000505288.1:p.Leu3528=
ENST00000265104.4:c.10627T= ENSP00000265104.4:p.Leu3543=
NM_001369.2:c.10627T= NP_001360.1:p.Leu3543=
XM_005248262.2:c.10582T= XP_005248319.1:p.Leu3528=
XM_005248262.3:c.10735T= XP_005248319.2:p.Leu3579=
XM_017009177.1:c.10735T= XP_016864666.1:p.Leu3579=
XM_017009178.1:c.9640T= XP_016864667.1:p.Leu3214=
XM_017009179.2:c.9640T= XP_016864668.1:p.Leu3214=
XM_017009180.1:c.10735T= XP_016864669.1:p.Leu3579=
XM_017009181.1:c.10735T= XP_016864670.1:p.Leu3579=
XM_017009182.1:c.10735T= XP_016864671.1:p.Leu3579=
XM_017009185.1:c.5824T= XP_016864674.1:p.Leu1942=
XM_017009186.1:c.5377T= XP_016864675.1:p.Leu1793=
XM_017009188.1:c.4714T= XP_016864677.1:p.Leu1572=
XM_024454388.1:c.9640T= XP_024310156.1:p.Leu3214=
XM_024454389.1:c.9229T= XP_024310157.1:p.Leu3077=
NM_001369.3:c.10627T= MANE Select NP_001360.1:p.Leu3543=