Canonical Allele Identifier: CA1528435443

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13776695T= , CM000667.2:g.13776695T=	GRCh38
NC_000005.9:g.13776804T= , CM000667.1:g.13776804T=	GRCh37
NC_000005.8:g.13829804T=	NCBI36
NG_013081.1:g.172786A=
NG_013081.2:g.172786A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.9117A= MANE Select	ENSP00000265104.4:p.Leu3039=
ENST00000681290.1:c.9072A=	ENSP00000505288.1:p.Leu3024=
ENST00000265104.4:c.9117A=	ENSP00000265104.4:p.Leu3039=
NM_001369.2:c.9117A=	NP_001360.1:p.Leu3039=
XM_005248262.2:c.9072A=	XP_005248319.1:p.Leu3024=
XM_011513990.1:c.*4A=	XP_011512292.1:n.*4A=
XR_925598.1:n.9188A=
XM_005248262.3:c.9225A=	XP_005248319.2:p.Leu3075=
XM_017009177.1:c.9225A=	XP_016864666.1:p.Leu3075=
XM_017009178.1:c.8130A=	XP_016864667.1:p.Leu2710=
XM_017009179.2:c.8130A=	XP_016864668.1:p.Leu2710=
XM_017009180.1:c.9225A=	XP_016864669.1:p.Leu3075=
XM_017009181.1:c.9225A=	XP_016864670.1:p.Leu3075=
XM_017009182.1:c.9225A=	XP_016864671.1:p.Leu3075=
XM_017009183.1:c.9225A=	XP_016864672.1:p.Leu3075=
XM_017009184.1:c.*4A=	XP_016864673.1:n.*4A=
XM_017009185.1:c.4314A=	XP_016864674.1:p.Leu1438=
XM_017009186.1:c.3867A=	XP_016864675.1:p.Leu1289=
XM_017009188.1:c.3204A=	XP_016864677.1:p.Leu1068=
XM_024454388.1:c.8130A=	XP_024310156.1:p.Leu2710=
XM_024454389.1:c.7719A=	XP_024310157.1:p.Leu2573=
XR_001742034.1:n.9111A=
XR_001742035.1:n.9106A=
NM_001369.3:c.9117A= MANE Select	NP_001360.1:p.Leu3039=