Canonical Allele Identifier: CA359219085
Community Standard Title: NM_001369.3(DNAH5):c.869G>A (p.Trp290Ter)
Gene: DNAH5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13919282C>T , CM000667.2:g.13919282C>T GRCh38
NC_000005.9:g.13919391C>T , CM000667.1:g.13919391C>T GRCh37
NC_000005.8:g.13972391C>T NCBI36
NG_013081.1:g.30199G>A
NG_013081.2:g.30199G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001369.3:c.869G>A MANE Select NP_001360.1:p.Trp290Ter
ENST00000265104.5:c.869G>A MANE Select ENSP00000265104.4:p.Trp290Ter
NM_001369.2:c.869G>A NP_001360.1:p.Trp290Ter
ENST00000265104.4:c.869G>A ENSP00000265104.4:p.Trp290Ter
ENST00000508040.1:n.1277G>A
ENST00000680213.1:c.629G>A ENSP00000506622.1:p.Trp210Ter
ENST00000680213.2:n.925G>A
ENST00000681290.1:c.824G>A ENSP00000505288.1:p.Trp275Ter
ENST00000682376.1:n.913G>A
ENST00000682586.1:n.962G>A
ENST00000683011.1:n.808G>A
ENST00000683967.1:n.968G>A
ENST00000684013.1:n.968G>A
ENST00000684099.1:n.964G>A
XM_005248262.2:c.824G>A XP_005248319.1:p.Trp275Ter
XM_005248262.3:c.977G>A XP_005248319.2:p.Trp326Ter
XM_011513990.1:c.869G>A XP_011512292.1:p.Trp290Ter
XM_017009177.1:c.977G>A XP_016864666.1:p.Trp326Ter
XM_017009178.1:c.-119G>A XP_016864667.1:n.-119G>A
XM_017009180.1:c.977G>A XP_016864669.1:p.Trp326Ter
XM_017009181.1:c.977G>A XP_016864670.1:p.Trp326Ter
XM_017009182.1:c.977G>A XP_016864671.1:p.Trp326Ter
XM_017009183.1:c.977G>A XP_016864672.1:p.Trp326Ter
XM_017009184.1:c.977G>A XP_016864673.1:p.Trp326Ter
XM_017009187.1:c.977G>A XP_016864676.1:p.Trp326Ter
XM_024454388.1:c.-2038G>A XP_024310156.1:n.-2038G>A
XM_024454389.1:c.-1091G>A XP_024310157.1:n.-1091G>A
XR_001742034.1:n.994G>A
XR_001742035.1:n.994G>A
XR_925598.1:n.1076G>A