Canonical Allele Identifier: CA1528458398

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13841812C= , CM000667.2:g.13841812C=	GRCh38
NC_000005.9:g.13841921C= , CM000667.1:g.13841921C=	GRCh37
NC_000005.8:g.13894921C=	NCBI36
NG_013081.1:g.107669G=
NG_013081.2:g.107669G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.5364G= MANE Select	ENSP00000265104.4:p.Trp1788=
ENST00000681290.1:c.5319G=	ENSP00000505288.1:p.Trp1773=
ENST00000265104.4:c.5364G=	ENSP00000265104.4:p.Trp1788=
NM_001369.2:c.5364G=	NP_001360.1:p.Trp1788=
XM_005248262.2:c.5319G=	XP_005248319.1:p.Trp1773=
XM_011513990.1:c.5364G=	XP_011512292.1:p.Trp1788=
XR_925598.1:n.5571G=
XM_005248262.3:c.5472G=	XP_005248319.2:p.Trp1824=
XM_017009177.1:c.5472G=	XP_016864666.1:p.Trp1824=
XM_017009178.1:c.4377G=	XP_016864667.1:p.Trp1459=
XM_017009179.2:c.4377G=	XP_016864668.1:p.Trp1459=
XM_017009180.1:c.5472G=	XP_016864669.1:p.Trp1824=
XM_017009181.1:c.5472G=	XP_016864670.1:p.Trp1824=
XM_017009182.1:c.5472G=	XP_016864671.1:p.Trp1824=
XM_017009183.1:c.5472G=	XP_016864672.1:p.Trp1824=
XM_017009184.1:c.5472G=	XP_016864673.1:p.Trp1824=
XM_017009185.1:c.561G=	XP_016864674.1:p.Trp187=
XM_017009186.1:c.114G=	XP_016864675.1:p.Trp38=
XM_017009187.1:c.5472G=	XP_016864676.1:p.Trp1824=
XM_024454388.1:c.4377G=	XP_024310156.1:p.Trp1459=
XM_024454389.1:c.3966G=	XP_024310157.1:p.Trp1322=
XR_001742034.1:n.5489G=
XR_001742035.1:n.5489G=
NM_001369.3:c.5364G= MANE Select	NP_001360.1:p.Trp1788=