Canonical Allele Identifier: CA1528441831

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13793946C= , CM000667.2:g.13793946C=	GRCh38
NC_000005.9:g.13794055C= , CM000667.1:g.13794055C=	GRCh37
NC_000005.8:g.13847055C=	NCBI36
NG_013081.1:g.155535G=
NG_013081.2:g.155535G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000265104.5:c.8000G= MANE Select	ENSP00000265104.4:p.Trp2667=
ENST00000681290.1:c.7955G=	ENSP00000505288.1:p.Trp2652=
ENST00000265104.4:c.8000G=	ENSP00000265104.4:p.Trp2667=
NM_001369.2:c.8000G=	NP_001360.1:p.Trp2667=
XM_005248262.2:c.7955G=	XP_005248319.1:p.Trp2652=
XM_011513990.1:c.8000G=	XP_011512292.1:p.Trp2667=
XR_925598.1:n.8207G=
XM_005248262.3:c.8108G=	XP_005248319.2:p.Trp2703=
XM_017009177.1:c.8108G=	XP_016864666.1:p.Trp2703=
XM_017009178.1:c.7013G=	XP_016864667.1:p.Trp2338=
XM_017009179.2:c.7013G=	XP_016864668.1:p.Trp2338=
XM_017009180.1:c.8108G=	XP_016864669.1:p.Trp2703=
XM_017009181.1:c.8108G=	XP_016864670.1:p.Trp2703=
XM_017009182.1:c.8108G=	XP_016864671.1:p.Trp2703=
XM_017009183.1:c.8108G=	XP_016864672.1:p.Trp2703=
XM_017009184.1:c.8108G=	XP_016864673.1:p.Trp2703=
XM_017009185.1:c.3197G=	XP_016864674.1:p.Trp1066=
XM_017009186.1:c.2750G=	XP_016864675.1:p.Trp917=
XM_017009188.1:c.2087G=	XP_016864677.1:p.Trp696=
XM_024454388.1:c.7013G=	XP_024310156.1:p.Trp2338=
XM_024454389.1:c.6602G=	XP_024310157.1:p.Trp2201=
XR_001742034.1:n.8125G=
XR_001742035.1:n.8125G=
NM_001369.3:c.8000G= MANE Select	NP_001360.1:p.Trp2667=