Canonical Allele Identifier: CA359220924
Gene: DNAH5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13793538T>A , CM000667.2:g.13793538T>A GRCh38
NC_000005.9:g.13793647T>A , CM000667.1:g.13793647T>A GRCh37
NC_000005.8:g.13846647T>A NCBI36
NG_013081.1:g.155943A>T
NG_013081.2:g.155943A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000265104.5:c.8201A>T MANE Select ENSP00000265104.4:p.Glu2734Val
ENST00000681290.1:c.8156A>T ENSP00000505288.1:p.Glu2719Val
ENST00000265104.4:c.8201A>T ENSP00000265104.4:p.Glu2734Val
NM_001369.2:c.8201A>T NP_001360.1:p.Glu2734Val
XM_005248262.2:c.8156A>T XP_005248319.1:p.Glu2719Val
XM_011513990.1:c.8201A>T XP_011512292.1:p.Glu2734Val
XR_925598.1:n.8408A>T
XM_005248262.3:c.8309A>T XP_005248319.2:p.Glu2770Val
XM_017009177.1:c.8309A>T XP_016864666.1:p.Glu2770Val
XM_017009178.1:c.7214A>T XP_016864667.1:p.Glu2405Val
XM_017009179.2:c.7214A>T XP_016864668.1:p.Glu2405Val
XM_017009180.1:c.8309A>T XP_016864669.1:p.Glu2770Val
XM_017009181.1:c.8309A>T XP_016864670.1:p.Glu2770Val
XM_017009182.1:c.8309A>T XP_016864671.1:p.Glu2770Val
XM_017009183.1:c.8309A>T XP_016864672.1:p.Glu2770Val
XM_017009184.1:c.8309A>T XP_016864673.1:p.Glu2770Val
XM_017009185.1:c.3398A>T XP_016864674.1:p.Glu1133Val
XM_017009186.1:c.2951A>T XP_016864675.1:p.Glu984Val
XM_017009188.1:c.2288A>T XP_016864677.1:p.Glu763Val
XM_024454388.1:c.7214A>T XP_024310156.1:p.Glu2405Val
XM_024454389.1:c.6803A>T XP_024310157.1:p.Glu2268Val
XR_001742034.1:n.8326A>T
XR_001742035.1:n.8326A>T
NM_001369.3:c.8201A>T MANE Select NP_001360.1:p.Glu2734Val