Canonical Allele Identifier: CA359211701
Gene: DNAH5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13841801A>C , CM000667.2:g.13841801A>C GRCh38
NC_000005.9:g.13841910A>C , CM000667.1:g.13841910A>C GRCh37
NC_000005.8:g.13894910A>C NCBI36
NG_013081.1:g.107680T>G
NG_013081.2:g.107680T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000265104.5:c.5375T>G MANE Select ENSP00000265104.4:p.Leu1792Arg
ENST00000681290.1:c.5330T>G ENSP00000505288.1:p.Leu1777Arg
ENST00000265104.4:c.5375T>G ENSP00000265104.4:p.Leu1792Arg
NM_001369.2:c.5375T>G NP_001360.1:p.Leu1792Arg
XM_005248262.2:c.5330T>G XP_005248319.1:p.Leu1777Arg
XM_011513990.1:c.5375T>G XP_011512292.1:p.Leu1792Arg
XR_925598.1:n.5582T>G
XM_005248262.3:c.5483T>G XP_005248319.2:p.Leu1828Arg
XM_017009177.1:c.5483T>G XP_016864666.1:p.Leu1828Arg
XM_017009178.1:c.4388T>G XP_016864667.1:p.Leu1463Arg
XM_017009179.2:c.4388T>G XP_016864668.1:p.Leu1463Arg
XM_017009180.1:c.5483T>G XP_016864669.1:p.Leu1828Arg
XM_017009181.1:c.5483T>G XP_016864670.1:p.Leu1828Arg
XM_017009182.1:c.5483T>G XP_016864671.1:p.Leu1828Arg
XM_017009183.1:c.5483T>G XP_016864672.1:p.Leu1828Arg
XM_017009184.1:c.5483T>G XP_016864673.1:p.Leu1828Arg
XM_017009185.1:c.572T>G XP_016864674.1:p.Leu191Arg
XM_017009186.1:c.125T>G XP_016864675.1:p.Leu42Arg
XM_017009187.1:c.5483T>G XP_016864676.1:p.Leu1828Arg
XM_024454388.1:c.4388T>G XP_024310156.1:p.Leu1463Arg
XM_024454389.1:c.3977T>G XP_024310157.1:p.Leu1326Arg
XR_001742034.1:n.5500T>G
XR_001742035.1:n.5500T>G
NM_001369.3:c.5375T>G MANE Select NP_001360.1:p.Leu1792Arg