Canonical Allele Identifier: CA1528403785

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13708268T= , CM000667.2:g.13708268T=	GRCh38
NC_000005.9:g.13708377T= , CM000667.1:g.13708377T=	GRCh37
NC_000005.8:g.13761377T=	NCBI36
NG_013081.1:g.241213A=
NG_013081.2:g.241213A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683611.1:n.526A=
ENST00000265104.5:c.13193A= MANE Select	ENSP00000265104.4:p.Asp4398=
ENST00000681290.1:c.13148A=	ENSP00000505288.1:p.Asp4383=
ENST00000265104.4:c.13193A=	ENSP00000265104.4:p.Asp4398=
NM_001369.2:c.13193A=	NP_001360.1:p.Asp4398=
XM_005248262.2:c.13148A=	XP_005248319.1:p.Asp4383=
XM_005248262.3:c.13301A=	XP_005248319.2:p.Asp4434=
XM_017009177.1:c.12881A=	XP_016864666.1:p.Asp4294=
XM_017009178.1:c.12206A=	XP_016864667.1:p.Asp4069=
XM_017009179.2:c.12206A=	XP_016864668.1:p.Asp4069=
XM_017009185.1:c.8390A=	XP_016864674.1:p.Asp2797=
XM_017009186.1:c.7943A=	XP_016864675.1:p.Asp2648=
XM_017009188.1:c.7280A=	XP_016864677.1:p.Asp2427=
XM_024454388.1:c.12206A=	XP_024310156.1:p.Asp4069=
XM_024454389.1:c.11795A=	XP_024310157.1:p.Asp3932=
NM_001369.3:c.13193A= MANE Select	NP_001360.1:p.Asp4398=