Canonical Allele Identifier: CA1528462619

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13839312G= , CM000667.2:g.13839312G=	GRCh38
NC_000005.9:g.13839421G= , CM000667.1:g.13839421G=	GRCh37
NC_000005.8:g.13892421G=	NCBI36
NG_013081.1:g.110169C=
NG_013081.2:g.110169C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.5882+44C= MANE Select	ENSP00000265104.4:n.5882+44C=
ENST00000681290.1:c.5837+44C=	ENSP00000505288.1:n.5837+44C=
ENST00000265104.4:c.5882+44C=	ENSP00000265104.4:n.5882+44C=
NM_001369.2:c.5882+44C=	NP_001360.1:n.5882+44C=
XM_005248262.2:c.5837+44C=	XP_005248319.1:n.5837+44C=
XM_011513990.1:c.5882+44C=	XP_011512292.1:n.5882+44C=
XR_925598.1:n.6089+44C=
XM_005248262.3:c.5990+44C=	XP_005248319.2:n.5990+44C=
XM_017009177.1:c.5990+44C=	XP_016864666.1:n.5990+44C=
XM_017009178.1:c.4895+44C=	XP_016864667.1:n.4895+44C=
XM_017009179.2:c.4895+44C=	XP_016864668.1:n.4895+44C=
XM_017009180.1:c.5990+44C=	XP_016864669.1:n.5990+44C=
XM_017009181.1:c.5990+44C=	XP_016864670.1:n.5990+44C=
XM_017009182.1:c.5990+44C=	XP_016864671.1:n.5990+44C=
XM_017009183.1:c.5990+44C=	XP_016864672.1:n.5990+44C=
XM_017009184.1:c.5990+44C=	XP_016864673.1:n.5990+44C=
XM_017009185.1:c.1079+44C=	XP_016864674.1:n.1079+44C=
XM_017009186.1:c.632+44C=	XP_016864675.1:n.632+44C=
XM_017009187.1:c.5990+44C=	XP_016864676.1:n.5990+44C=
XM_024454388.1:c.4895+44C=	XP_024310156.1:n.4895+44C=
XM_024454389.1:c.4484+44C=	XP_024310157.1:n.4484+44C=
XR_001742034.1:n.6007+44C=
XR_001742035.1:n.6007+44C=
NM_001369.3:c.5882+44C= MANE Select	NP_001360.1:n.5882+44C=