Canonical Allele Identifier: CA359205523
Gene: DNAH5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13901398T>A , CM000667.2:g.13901398T>A GRCh38
NC_000005.9:g.13901507T>A , CM000667.1:g.13901507T>A GRCh37
NC_000005.8:g.13954507T>A NCBI36
NG_013081.1:g.48083A>T
NG_013081.2:g.48083A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000265104.5:c.1906A>T MANE Select ENSP00000265104.4:p.Arg636Trp
ENST00000681290.1:c.1861A>T ENSP00000505288.1:p.Arg621Trp
ENST00000265104.4:c.1906A>T ENSP00000265104.4:p.Arg636Trp
NM_001369.2:c.1906A>T NP_001360.1:p.Arg636Trp
XM_005248262.2:c.1861A>T XP_005248319.1:p.Arg621Trp
XM_011513990.1:c.1906A>T XP_011512292.1:p.Arg636Trp
XR_925598.1:n.2113A>T
XM_005248262.3:c.2014A>T XP_005248319.2:p.Arg672Trp
XM_017009177.1:c.2014A>T XP_016864666.1:p.Arg672Trp
XM_017009178.1:c.919A>T XP_016864667.1:p.Arg307Trp
XM_017009179.2:c.919A>T XP_016864668.1:p.Arg307Trp
XM_017009180.1:c.2014A>T XP_016864669.1:p.Arg672Trp
XM_017009181.1:c.2014A>T XP_016864670.1:p.Arg672Trp
XM_017009182.1:c.2014A>T XP_016864671.1:p.Arg672Trp
XM_017009183.1:c.2014A>T XP_016864672.1:p.Arg672Trp
XM_017009184.1:c.2014A>T XP_016864673.1:p.Arg672Trp
XM_017009187.1:c.2014A>T XP_016864676.1:p.Arg672Trp
XM_024454388.1:c.919A>T XP_024310156.1:p.Arg307Trp
XM_024454389.1:c.508A>T XP_024310157.1:p.Arg170Trp
XR_001742034.1:n.2031A>T
XR_001742035.1:n.2031A>T
NM_001369.3:c.1906A>T MANE Select NP_001360.1:p.Arg636Trp