Canonical Allele Identifier: CA1528422972

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13752274G= , CM000667.2:g.13752274G=	GRCh38
NC_000005.9:g.13752383G= , CM000667.1:g.13752383G=	GRCh37
NC_000005.8:g.13805383G=	NCBI36
NG_013081.1:g.197207C=
NG_013081.2:g.197207C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.10888C= MANE Select	ENSP00000265104.4:p.His3630=
ENST00000681290.1:c.10843C=	ENSP00000505288.1:p.His3615=
ENST00000265104.4:c.10888C=	ENSP00000265104.4:p.His3630=
NM_001369.2:c.10888C=	NP_001360.1:p.His3630=
XM_005248262.2:c.10843C=	XP_005248319.1:p.His3615=
XM_005248262.3:c.10996C=	XP_005248319.2:p.His3666=
XM_017009177.1:c.10996C=	XP_016864666.1:p.His3666=
XM_017009178.1:c.9901C=	XP_016864667.1:p.His3301=
XM_017009179.2:c.9901C=	XP_016864668.1:p.His3301=
XM_017009180.1:c.10996C=	XP_016864669.1:p.His3666=
XM_017009181.1:c.10996C=	XP_016864670.1:p.His3666=
XM_017009182.1:c.10996C=	XP_016864671.1:p.His3666=
XM_017009185.1:c.6085C=	XP_016864674.1:p.His2029=
XM_017009186.1:c.5638C=	XP_016864675.1:p.His1880=
XM_017009188.1:c.4975C=	XP_016864677.1:p.His1659=
XM_024454388.1:c.9901C=	XP_024310156.1:p.His3301=
XM_024454389.1:c.9490C=	XP_024310157.1:p.His3164=
NM_001369.3:c.10888C= MANE Select	NP_001360.1:p.His3630=