Canonical Allele Identifier: CA359211783
Gene: DNAH5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13841813C>A , CM000667.2:g.13841813C>A GRCh38
NC_000005.9:g.13841922C>A , CM000667.1:g.13841922C>A GRCh37
NC_000005.8:g.13894922C>A NCBI36
NG_013081.1:g.107668G>T
NG_013081.2:g.107668G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000265104.5:c.5363G>T MANE Select ENSP00000265104.4:p.Trp1788Leu
ENST00000681290.1:c.5318G>T ENSP00000505288.1:p.Trp1773Leu
ENST00000265104.4:c.5363G>T ENSP00000265104.4:p.Trp1788Leu
NM_001369.2:c.5363G>T NP_001360.1:p.Trp1788Leu
XM_005248262.2:c.5318G>T XP_005248319.1:p.Trp1773Leu
XM_011513990.1:c.5363G>T XP_011512292.1:p.Trp1788Leu
XR_925598.1:n.5570G>T
XM_005248262.3:c.5471G>T XP_005248319.2:p.Trp1824Leu
XM_017009177.1:c.5471G>T XP_016864666.1:p.Trp1824Leu
XM_017009178.1:c.4376G>T XP_016864667.1:p.Trp1459Leu
XM_017009179.2:c.4376G>T XP_016864668.1:p.Trp1459Leu
XM_017009180.1:c.5471G>T XP_016864669.1:p.Trp1824Leu
XM_017009181.1:c.5471G>T XP_016864670.1:p.Trp1824Leu
XM_017009182.1:c.5471G>T XP_016864671.1:p.Trp1824Leu
XM_017009183.1:c.5471G>T XP_016864672.1:p.Trp1824Leu
XM_017009184.1:c.5471G>T XP_016864673.1:p.Trp1824Leu
XM_017009185.1:c.560G>T XP_016864674.1:p.Trp187Leu
XM_017009186.1:c.113G>T XP_016864675.1:p.Trp38Leu
XM_017009187.1:c.5471G>T XP_016864676.1:p.Trp1824Leu
XM_024454388.1:c.4376G>T XP_024310156.1:p.Trp1459Leu
XM_024454389.1:c.3965G>T XP_024310157.1:p.Trp1322Leu
XR_001742034.1:n.5488G>T
XR_001742035.1:n.5488G>T
NM_001369.3:c.5363G>T MANE Select NP_001360.1:p.Trp1788Leu