Canonical Allele Identifier: CA1528423520

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13753459T= , CM000667.2:g.13753459T=	GRCh38
NC_000005.9:g.13753568T= , CM000667.1:g.13753568T=	GRCh37
NC_000005.8:g.13806568T=	NCBI36
NG_013081.1:g.196022A=
NG_013081.2:g.196022A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.10646A= MANE Select	ENSP00000265104.4:p.Glu3549=
ENST00000681290.1:c.10601A=	ENSP00000505288.1:p.Glu3534=
ENST00000265104.4:c.10646A=	ENSP00000265104.4:p.Glu3549=
NM_001369.2:c.10646A=	NP_001360.1:p.Glu3549=
XM_005248262.2:c.10601A=	XP_005248319.1:p.Glu3534=
XM_005248262.3:c.10754A=	XP_005248319.2:p.Glu3585=
XM_017009177.1:c.10754A=	XP_016864666.1:p.Glu3585=
XM_017009178.1:c.9659A=	XP_016864667.1:p.Glu3220=
XM_017009179.2:c.9659A=	XP_016864668.1:p.Glu3220=
XM_017009180.1:c.10754A=	XP_016864669.1:p.Glu3585=
XM_017009181.1:c.10754A=	XP_016864670.1:p.Glu3585=
XM_017009182.1:c.10754A=	XP_016864671.1:p.Glu3585=
XM_017009185.1:c.5843A=	XP_016864674.1:p.Glu1948=
XM_017009186.1:c.5396A=	XP_016864675.1:p.Glu1799=
XM_017009188.1:c.4733A=	XP_016864677.1:p.Glu1578=
XM_024454388.1:c.9659A=	XP_024310156.1:p.Glu3220=
XM_024454389.1:c.9248A=	XP_024310157.1:p.Glu3083=
NM_001369.3:c.10646A= MANE Select	NP_001360.1:p.Glu3549=