Canonical Allele Identifier: CA1073399202
Gene: DNAH5 HGNC NCBI

Linked Data

dbSNP Id: rs1757011763

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13791677del , CM000667.2:g.13791677del GRCh38
NC_000005.9:g.13791786del , CM000667.1:g.13791786del GRCh37
NC_000005.8:g.13844786del NCBI36
NG_013081.1:g.157806del
NG_013081.2:g.157806del

Transcript Alleles

HGVS Amino-acid Change
ENST00000265104.5:c.8448+319del MANE Select ENSP00000265104.4:n.8448+319del
ENST00000681290.1:c.8403+319del ENSP00000505288.1:n.8403+319del
ENST00000265104.4:c.8448+319del ENSP00000265104.4:n.8448+319del
NM_001369.2:c.8448+319del NP_001360.1:n.8448+319del
XM_005248262.2:c.8403+319del XP_005248319.1:n.8403+319del
XM_011513990.1:c.8448+319del XP_011512292.1:n.8448+319del
XR_925598.1:n.8655+319del
XM_005248262.3:c.8556+319del XP_005248319.2:n.8556+319del
XM_017009177.1:c.8556+319del XP_016864666.1:n.8556+319del
XM_017009178.1:c.7461+319del XP_016864667.1:n.7461+319del
XM_017009179.2:c.7461+319del XP_016864668.1:n.7461+319del
XM_017009180.1:c.8556+319del XP_016864669.1:n.8556+319del
XM_017009181.1:c.8556+319del XP_016864670.1:n.8556+319del
XM_017009182.1:c.8556+319del XP_016864671.1:n.8556+319del
XM_017009183.1:c.8556+319del XP_016864672.1:n.8556+319del
XM_017009184.1:c.8556+319del XP_016864673.1:n.8556+319del
XM_017009185.1:c.3645+319del XP_016864674.1:n.3645+319del
XM_017009186.1:c.3198+319del XP_016864675.1:n.3198+319del
XM_017009188.1:c.2535+319del XP_016864677.1:n.2535+319del
XM_024454388.1:c.7461+319del XP_024310156.1:n.7461+319del
XM_024454389.1:c.7050+319del XP_024310157.1:n.7050+319del
XR_001742034.1:n.8573+319del
XR_001742035.1:n.8573+319del
NM_001369.3:c.8448+319del MANE Select NP_001360.1:n.8448+319del