Canonical Allele Identifier: CA1528476319

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13870803C= , CM000667.2:g.13870803C=	GRCh38
NC_000005.9:g.13870912C= , CM000667.1:g.13870912C=	GRCh37
NC_000005.8:g.13923912C=	NCBI36
NG_013081.1:g.78678G=
NG_013081.2:g.78678G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.3798G= MANE Select	ENSP00000265104.4:p.Glu1266=
ENST00000681290.1:c.3753G=	ENSP00000505288.1:p.Glu1251=
ENST00000265104.4:c.3798G=	ENSP00000265104.4:p.Glu1266=
NM_001369.2:c.3798G=	NP_001360.1:p.Glu1266=
XM_005248262.2:c.3753G=	XP_005248319.1:p.Glu1251=
XM_011513990.1:c.3798G=	XP_011512292.1:p.Glu1266=
XR_925598.1:n.4005G=
XM_005248262.3:c.3906G=	XP_005248319.2:p.Glu1302=
XM_017009177.1:c.3906G=	XP_016864666.1:p.Glu1302=
XM_017009178.1:c.2811G=	XP_016864667.1:p.Glu937=
XM_017009179.2:c.2811G=	XP_016864668.1:p.Glu937=
XM_017009180.1:c.3906G=	XP_016864669.1:p.Glu1302=
XM_017009181.1:c.3906G=	XP_016864670.1:p.Glu1302=
XM_017009182.1:c.3906G=	XP_016864671.1:p.Glu1302=
XM_017009183.1:c.3906G=	XP_016864672.1:p.Glu1302=
XM_017009184.1:c.3906G=	XP_016864673.1:p.Glu1302=
XM_017009187.1:c.3906G=	XP_016864676.1:p.Glu1302=
XM_024454388.1:c.2811G=	XP_024310156.1:p.Glu937=
XM_024454389.1:c.2400G=	XP_024310157.1:p.Glu800=
XR_001742034.1:n.3923G=
XR_001742035.1:n.3923G=
NM_001369.3:c.3798G= MANE Select	NP_001360.1:p.Glu1266=