Canonical Allele Identifier: CA1528462660

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13839375T= , CM000667.2:g.13839375T=	GRCh38
NC_000005.9:g.13839484T= , CM000667.1:g.13839484T=	GRCh37
NC_000005.8:g.13892484T=	NCBI36
NG_013081.1:g.110106A=
NG_013081.2:g.110106A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.5863A= MANE Select	ENSP00000265104.4:p.Ile1955=
ENST00000681290.1:c.5818A=	ENSP00000505288.1:p.Ile1940=
ENST00000265104.4:c.5863A=	ENSP00000265104.4:p.Ile1955=
NM_001369.2:c.5863A=	NP_001360.1:p.Ile1955=
XM_005248262.2:c.5818A=	XP_005248319.1:p.Ile1940=
XM_011513990.1:c.5863A=	XP_011512292.1:p.Ile1955=
XR_925598.1:n.6070A=
XM_005248262.3:c.5971A=	XP_005248319.2:p.Ile1991=
XM_017009177.1:c.5971A=	XP_016864666.1:p.Ile1991=
XM_017009178.1:c.4876A=	XP_016864667.1:p.Ile1626=
XM_017009179.2:c.4876A=	XP_016864668.1:p.Ile1626=
XM_017009180.1:c.5971A=	XP_016864669.1:p.Ile1991=
XM_017009181.1:c.5971A=	XP_016864670.1:p.Ile1991=
XM_017009182.1:c.5971A=	XP_016864671.1:p.Ile1991=
XM_017009183.1:c.5971A=	XP_016864672.1:p.Ile1991=
XM_017009184.1:c.5971A=	XP_016864673.1:p.Ile1991=
XM_017009185.1:c.1060A=	XP_016864674.1:p.Ile354=
XM_017009186.1:c.613A=	XP_016864675.1:p.Ile205=
XM_017009187.1:c.5971A=	XP_016864676.1:p.Ile1991=
XM_024454388.1:c.4876A=	XP_024310156.1:p.Ile1626=
XM_024454389.1:c.4465A=	XP_024310157.1:p.Ile1489=
XR_001742034.1:n.5988A=
XR_001742035.1:n.5988A=
NM_001369.3:c.5863A= MANE Select	NP_001360.1:p.Ile1955=