Canonical Allele Identifier: CA1528441647

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13793571T= , CM000667.2:g.13793571T=	GRCh38
NC_000005.9:g.13793680T= , CM000667.1:g.13793680T=	GRCh37
NC_000005.8:g.13846680T=	NCBI36
NG_013081.1:g.155910A=
NG_013081.2:g.155910A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.8168A= MANE Select	ENSP00000265104.4:p.Gln2723=
ENST00000681290.1:c.8123A=	ENSP00000505288.1:p.Gln2708=
ENST00000265104.4:c.8168A=	ENSP00000265104.4:p.Gln2723=
NM_001369.2:c.8168A=	NP_001360.1:p.Gln2723=
XM_005248262.2:c.8123A=	XP_005248319.1:p.Gln2708=
XM_011513990.1:c.8168A=	XP_011512292.1:p.Gln2723=
XR_925598.1:n.8375A=
XM_005248262.3:c.8276A=	XP_005248319.2:p.Gln2759=
XM_017009177.1:c.8276A=	XP_016864666.1:p.Gln2759=
XM_017009178.1:c.7181A=	XP_016864667.1:p.Gln2394=
XM_017009179.2:c.7181A=	XP_016864668.1:p.Gln2394=
XM_017009180.1:c.8276A=	XP_016864669.1:p.Gln2759=
XM_017009181.1:c.8276A=	XP_016864670.1:p.Gln2759=
XM_017009182.1:c.8276A=	XP_016864671.1:p.Gln2759=
XM_017009183.1:c.8276A=	XP_016864672.1:p.Gln2759=
XM_017009184.1:c.8276A=	XP_016864673.1:p.Gln2759=
XM_017009185.1:c.3365A=	XP_016864674.1:p.Gln1122=
XM_017009186.1:c.2918A=	XP_016864675.1:p.Gln973=
XM_017009188.1:c.2255A=	XP_016864677.1:p.Gln752=
XM_024454388.1:c.7181A=	XP_024310156.1:p.Gln2394=
XM_024454389.1:c.6770A=	XP_024310157.1:p.Gln2257=
XR_001742034.1:n.8293A=
XR_001742035.1:n.8293A=
NM_001369.3:c.8168A= MANE Select	NP_001360.1:p.Gln2723=