Canonical Allele Identifier: CA3203945
Community Standard Title: NM_001369.3(DNAH5):c.4587G>A (p.Glu1529=)
Gene: DNAH5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13864406C>T , CM000667.2:g.13864406C>T GRCh38
NC_000005.9:g.13864515C>T , CM000667.1:g.13864515C>T GRCh37
NC_000005.8:g.13917515C>T NCBI36
NG_013081.1:g.85075G>A
NG_013081.2:g.85075G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001369.3:c.4587G>A MANE Select NP_001360.1:p.Glu1529=
ENST00000265104.5:c.4587G>A MANE Select ENSP00000265104.4:p.Glu1529=
NM_001369.2:c.4587G>A NP_001360.1:p.Glu1529=
ENST00000265104.4:c.4587G>A ENSP00000265104.4:p.Glu1529=
ENST00000681290.1:c.4542G>A ENSP00000505288.1:p.Glu1514=
XM_005248262.2:c.4542G>A XP_005248319.1:p.Glu1514=
XM_005248262.3:c.4695G>A XP_005248319.2:p.Glu1565=
XM_011513990.1:c.4587G>A XP_011512292.1:p.Glu1529=
XM_017009177.1:c.4695G>A XP_016864666.1:p.Glu1565=
XM_017009178.1:c.3600G>A XP_016864667.1:p.Glu1200=
XM_017009179.2:c.3600G>A XP_016864668.1:p.Glu1200=
XM_017009180.1:c.4695G>A XP_016864669.1:p.Glu1565=
XM_017009181.1:c.4695G>A XP_016864670.1:p.Glu1565=
XM_017009182.1:c.4695G>A XP_016864671.1:p.Glu1565=
XM_017009183.1:c.4695G>A XP_016864672.1:p.Glu1565=
XM_017009184.1:c.4695G>A XP_016864673.1:p.Glu1565=
XM_017009187.1:c.4695G>A XP_016864676.1:p.Glu1565=
XM_024454388.1:c.3600G>A XP_024310156.1:p.Glu1200=
XM_024454389.1:c.3189G>A XP_024310157.1:p.Glu1063=
XR_001742034.1:n.4712G>A
XR_001742035.1:n.4712G>A
XR_925598.1:n.4794G>A