Canonical Allele Identifier: CA3203631

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13841007A>G , CM000667.2:g.13841007A>G	GRCh38
NC_000005.9:g.13841116A>G , CM000667.1:g.13841116A>G	GRCh37
NC_000005.8:g.13894116A>G	NCBI36
NG_013081.1:g.108474T>C
NG_013081.2:g.108474T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001369.3:c.5608T>C MANE Select	NP_001360.1:p.Leu1870=
ENST00000265104.5:c.5608T>C MANE Select	ENSP00000265104.4:p.Leu1870=
NM_001369.2:c.5608T>C	NP_001360.1:p.Leu1870=
ENST00000265104.4:c.5608T>C	ENSP00000265104.4:p.Leu1870=
ENST00000681290.1:c.5563T>C	ENSP00000505288.1:p.Leu1855=
XM_005248262.2:c.5563T>C	XP_005248319.1:p.Leu1855=
XM_005248262.3:c.5716T>C	XP_005248319.2:p.Leu1906=
XM_011513990.1:c.5608T>C	XP_011512292.1:p.Leu1870=
XM_017009177.1:c.5716T>C	XP_016864666.1:p.Leu1906=
XM_017009178.1:c.4621T>C	XP_016864667.1:p.Leu1541=
XM_017009179.2:c.4621T>C	XP_016864668.1:p.Leu1541=
XM_017009180.1:c.5716T>C	XP_016864669.1:p.Leu1906=
XM_017009181.1:c.5716T>C	XP_016864670.1:p.Leu1906=
XM_017009182.1:c.5716T>C	XP_016864671.1:p.Leu1906=
XM_017009183.1:c.5716T>C	XP_016864672.1:p.Leu1906=
XM_017009184.1:c.5716T>C	XP_016864673.1:p.Leu1906=
XM_017009185.1:c.805T>C	XP_016864674.1:p.Leu269=
XM_017009186.1:c.358T>C	XP_016864675.1:p.Leu120=
XM_017009187.1:c.5716T>C	XP_016864676.1:p.Leu1906=
XM_024454388.1:c.4621T>C	XP_024310156.1:p.Leu1541=
XM_024454389.1:c.4210T>C	XP_024310157.1:p.Leu1404=
XR_001742034.1:n.5733T>C
XR_001742035.1:n.5733T>C
XR_925598.1:n.5815T>C