Canonical Allele Identifier: CA1528403784

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13708267G= , CM000667.2:g.13708267G=	GRCh38
NC_000005.9:g.13708376G= , CM000667.1:g.13708376G=	GRCh37
NC_000005.8:g.13761376G=	NCBI36
NG_013081.1:g.241214C=
NG_013081.2:g.241214C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000683611.1:n.527C=
ENST00000265104.5:c.13194C= MANE Select	ENSP00000265104.4:p.Asp4398=
ENST00000681290.1:c.13149C=	ENSP00000505288.1:p.Asp4383=
ENST00000265104.4:c.13194C=	ENSP00000265104.4:p.Asp4398=
NM_001369.2:c.13194C=	NP_001360.1:p.Asp4398=
XM_005248262.2:c.13149C=	XP_005248319.1:p.Asp4383=
XM_005248262.3:c.13302C=	XP_005248319.2:p.Asp4434=
XM_017009177.1:c.12882C=	XP_016864666.1:p.Asp4294=
XM_017009178.1:c.12207C=	XP_016864667.1:p.Asp4069=
XM_017009179.2:c.12207C=	XP_016864668.1:p.Asp4069=
XM_017009185.1:c.8391C=	XP_016864674.1:p.Asp2797=
XM_017009186.1:c.7944C=	XP_016864675.1:p.Asp2648=
XM_017009188.1:c.7281C=	XP_016864677.1:p.Asp2427=
XM_024454388.1:c.12207C=	XP_024310156.1:p.Asp4069=
XM_024454389.1:c.11796C=	XP_024310157.1:p.Asp3932=
NM_001369.3:c.13194C= MANE Select	NP_001360.1:p.Asp4398=