Canonical Allele Identifier: CA1528415097

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13735819T= , CM000667.2:g.13735819T=	GRCh38
NC_000005.9:g.13735928T= , CM000667.1:g.13735928T=	GRCh37
NC_000005.8:g.13788928T=	NCBI36
NG_013081.1:g.213662A=
NG_013081.2:g.213662A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000265104.5:c.11569A= MANE Select	ENSP00000265104.4:p.Arg3857=
ENST00000681290.1:c.11524A=	ENSP00000505288.1:p.Arg3842=
ENST00000265104.4:c.11569A=	ENSP00000265104.4:p.Arg3857=
NM_001369.2:c.11569A=	NP_001360.1:p.Arg3857=
XM_005248262.2:c.11524A=	XP_005248319.1:p.Arg3842=
XM_005248262.3:c.11677A=	XP_005248319.2:p.Arg3893=
XM_017009177.1:c.11677A=	XP_016864666.1:p.Arg3893=
XM_017009178.1:c.10582A=	XP_016864667.1:p.Arg3528=
XM_017009179.2:c.10582A=	XP_016864668.1:p.Arg3528=
XM_017009180.1:c.11677A=	XP_016864669.1:p.Arg3893=
XM_017009181.1:c.11677A=	XP_016864670.1:p.Arg3893=
XM_017009182.1:c.*3A=	XP_016864671.1:n.*3A=
XM_017009185.1:c.6766A=	XP_016864674.1:p.Arg2256=
XM_017009186.1:c.6319A=	XP_016864675.1:p.Arg2107=
XM_017009188.1:c.5656A=	XP_016864677.1:p.Arg1886=
XM_024454388.1:c.10582A=	XP_024310156.1:p.Arg3528=
XM_024454389.1:c.10171A=	XP_024310157.1:p.Arg3391=
NM_001369.3:c.11569A= MANE Select	NP_001360.1:p.Arg3857=