Canonical Allele Identifier: CA1528422971

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13752272G= , CM000667.2:g.13752272G=	GRCh38
NC_000005.9:g.13752381G= , CM000667.1:g.13752381G=	GRCh37
NC_000005.8:g.13805381G=	NCBI36
NG_013081.1:g.197209C=
NG_013081.2:g.197209C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.10890C= MANE Select	ENSP00000265104.4:p.His3630=
ENST00000681290.1:c.10845C=	ENSP00000505288.1:p.His3615=
ENST00000265104.4:c.10890C=	ENSP00000265104.4:p.His3630=
NM_001369.2:c.10890C=	NP_001360.1:p.His3630=
XM_005248262.2:c.10845C=	XP_005248319.1:p.His3615=
XM_005248262.3:c.10998C=	XP_005248319.2:p.His3666=
XM_017009177.1:c.10998C=	XP_016864666.1:p.His3666=
XM_017009178.1:c.9903C=	XP_016864667.1:p.His3301=
XM_017009179.2:c.9903C=	XP_016864668.1:p.His3301=
XM_017009180.1:c.10998C=	XP_016864669.1:p.His3666=
XM_017009181.1:c.10998C=	XP_016864670.1:p.His3666=
XM_017009182.1:c.10998C=	XP_016864671.1:p.His3666=
XM_017009185.1:c.6087C=	XP_016864674.1:p.His2029=
XM_017009186.1:c.5640C=	XP_016864675.1:p.His1880=
XM_017009188.1:c.4977C=	XP_016864677.1:p.His1659=
XM_024454388.1:c.9903C=	XP_024310156.1:p.His3301=
XM_024454389.1:c.9492C=	XP_024310157.1:p.His3164=
NM_001369.3:c.10890C= MANE Select	NP_001360.1:p.His3630=