Canonical Allele Identifier: CA1528440771
Gene: DNAH5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13791721_13791722delinsTA , CM000667.2:g.13791721_13791722delinsTA GRCh38
NC_000005.9:g.13791830_13791831delinsTA , CM000667.1:g.13791830_13791831delinsTA GRCh37
NC_000005.8:g.13844830_13844831delinsTA NCBI36
NG_013081.1:g.157759_157760delinsTA
NG_013081.2:g.157759_157760delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000265104.5:c.8448+272_8448+273delinsTA MANE Select ENSP00000265104.4:n.8448+272_8448+273delinsTA
ENST00000681290.1:c.8403+272_8403+273delinsTA ENSP00000505288.1:n.8403+272_8403+273delinsTA
ENST00000265104.4:c.8448+272_8448+273delinsTA ENSP00000265104.4:n.8448+272_8448+273delinsTA
NM_001369.2:c.8448+272_8448+273delinsTA NP_001360.1:n.8448+272_8448+273delinsTA
XM_005248262.2:c.8403+272_8403+273delinsTA XP_005248319.1:n.8403+272_8403+273delinsTA
XM_011513990.1:c.8448+272_8448+273delinsTA XP_011512292.1:n.8448+272_8448+273delinsTA
XR_925598.1:n.8655+272_8655+273delinsTA
XM_005248262.3:c.8556+272_8556+273delinsTA XP_005248319.2:n.8556+272_8556+273delinsTA
XM_017009177.1:c.8556+272_8556+273delinsTA XP_016864666.1:n.8556+272_8556+273delinsTA
XM_017009178.1:c.7461+272_7461+273delinsTA XP_016864667.1:n.7461+272_7461+273delinsTA
XM_017009179.2:c.7461+272_7461+273delinsTA XP_016864668.1:n.7461+272_7461+273delinsTA
XM_017009180.1:c.8556+272_8556+273delinsTA XP_016864669.1:n.8556+272_8556+273delinsTA
XM_017009181.1:c.8556+272_8556+273delinsTA XP_016864670.1:n.8556+272_8556+273delinsTA
XM_017009182.1:c.8556+272_8556+273delinsTA XP_016864671.1:n.8556+272_8556+273delinsTA
XM_017009183.1:c.8556+272_8556+273delinsTA XP_016864672.1:n.8556+272_8556+273delinsTA
XM_017009184.1:c.8556+272_8556+273delinsTA XP_016864673.1:n.8556+272_8556+273delinsTA
XM_017009185.1:c.3645+272_3645+273delinsTA XP_016864674.1:n.3645+272_3645+273delinsTA
XM_017009186.1:c.3198+272_3198+273delinsTA XP_016864675.1:n.3198+272_3198+273delinsTA
XM_017009188.1:c.2535+272_2535+273delinsTA XP_016864677.1:n.2535+272_2535+273delinsTA
XM_024454388.1:c.7461+272_7461+273delinsTA XP_024310156.1:n.7461+272_7461+273delinsTA
XM_024454389.1:c.7050+272_7050+273delinsTA XP_024310157.1:n.7050+272_7050+273delinsTA
XR_001742034.1:n.8573+272_8573+273delinsTA
XR_001742035.1:n.8573+272_8573+273delinsTA
NM_001369.3:c.8448+272_8448+273delinsTA MANE Select NP_001360.1:n.8448+272_8448+273delinsTA