Canonical Allele Identifier: CA1528483821

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13886049C= , CM000667.2:g.13886049C=	GRCh38
NC_000005.9:g.13886158C= , CM000667.1:g.13886158C=	GRCh37
NC_000005.8:g.13939158C=	NCBI36
NG_013081.1:g.63432G=
NG_013081.2:g.63432G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000265104.5:c.2658G= MANE Select	ENSP00000265104.4:p.Met886=
ENST00000681290.1:c.2613G=	ENSP00000505288.1:p.Met871=
ENST00000265104.4:c.2658G=	ENSP00000265104.4:p.Met886=
NM_001369.2:c.2658G=	NP_001360.1:p.Met886=
XM_005248262.2:c.2613G=	XP_005248319.1:p.Met871=
XM_011513990.1:c.2658G=	XP_011512292.1:p.Met886=
XR_925598.1:n.2865G=
XM_005248262.3:c.2766G=	XP_005248319.2:p.Met922=
XM_017009177.1:c.2766G=	XP_016864666.1:p.Met922=
XM_017009178.1:c.1671G=	XP_016864667.1:p.Met557=
XM_017009179.2:c.1671G=	XP_016864668.1:p.Met557=
XM_017009180.1:c.2766G=	XP_016864669.1:p.Met922=
XM_017009181.1:c.2766G=	XP_016864670.1:p.Met922=
XM_017009182.1:c.2766G=	XP_016864671.1:p.Met922=
XM_017009183.1:c.2766G=	XP_016864672.1:p.Met922=
XM_017009184.1:c.2766G=	XP_016864673.1:p.Met922=
XM_017009187.1:c.2766G=	XP_016864676.1:p.Met922=
XM_024454388.1:c.1671G=	XP_024310156.1:p.Met557=
XM_024454389.1:c.1260G=	XP_024310157.1:p.Met420=
XR_001742034.1:n.2783G=
XR_001742035.1:n.2783G=
NM_001369.3:c.2658G= MANE Select	NP_001360.1:p.Met886=