Canonical Allele Identifier: CA1528430359

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13769036G= , CM000667.2:g.13769036G=	GRCh38
NC_000005.9:g.13769145G= , CM000667.1:g.13769145G=	GRCh37
NC_000005.8:g.13822145G=	NCBI36
NG_013081.1:g.180445C=
NG_013081.2:g.180445C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.9821C= MANE Select	ENSP00000265104.4:p.Ser3274=
ENST00000681290.1:c.9776C=	ENSP00000505288.1:p.Ser3259=
ENST00000265104.4:c.9821C=	ENSP00000265104.4:p.Ser3274=
ENST00000504001.3:n.533C=
NM_001369.2:c.9821C=	NP_001360.1:p.Ser3274=
XM_005248262.2:c.9776C=	XP_005248319.1:p.Ser3259=
XM_005248262.3:c.9929C=	XP_005248319.2:p.Ser3310=
XM_017009177.1:c.9929C=	XP_016864666.1:p.Ser3310=
XM_017009178.1:c.8834C=	XP_016864667.1:p.Ser2945=
XM_017009179.2:c.8834C=	XP_016864668.1:p.Ser2945=
XM_017009180.1:c.9929C=	XP_016864669.1:p.Ser3310=
XM_017009181.1:c.9929C=	XP_016864670.1:p.Ser3310=
XM_017009182.1:c.9929C=	XP_016864671.1:p.Ser3310=
XM_017009185.1:c.5018C=	XP_016864674.1:p.Ser1673=
XM_017009186.1:c.4571C=	XP_016864675.1:p.Ser1524=
XM_017009188.1:c.3908C=	XP_016864677.1:p.Ser1303=
XM_024454388.1:c.8834C=	XP_024310156.1:p.Ser2945=
XM_024454389.1:c.8423C=	XP_024310157.1:p.Ser2808=
NM_001369.3:c.9821C= MANE Select	NP_001360.1:p.Ser3274=