Canonical Allele Identifier: CA1528399825

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13701166C= , CM000667.2:g.13701166C=	GRCh38
NC_000005.9:g.13701275C= , CM000667.1:g.13701275C=	GRCh37
NC_000005.8:g.13754275C=	NCBI36
NG_013081.1:g.248315G=
NG_013081.2:g.248315G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683611.1:n.824+118G=
ENST00000265104.5:c.13491+118G= MANE Select	ENSP00000265104.4:n.13491+118G=
ENST00000681290.1:c.13446+118G=	ENSP00000505288.1:n.13446+118G=
ENST00000265104.4:c.13491+118G=	ENSP00000265104.4:n.13491+118G=
NM_001369.2:c.13491+118G=	NP_001360.1:n.13491+118G=
XM_005248262.2:c.13446+118G=	XP_005248319.1:n.13446+118G=
XM_005248262.3:c.13599+118G=	XP_005248319.2:n.13599+118G=
XM_017009177.1:c.13179+118G=	XP_016864666.1:n.13179+118G=
XM_017009178.1:c.12504+118G=	XP_016864667.1:n.12504+118G=
XM_017009179.2:c.12504+118G=	XP_016864668.1:n.12504+118G=
XM_017009185.1:c.8688+118G=	XP_016864674.1:n.8688+118G=
XM_017009186.1:c.8241+118G=	XP_016864675.1:n.8241+118G=
XM_017009188.1:c.7578+118G=	XP_016864677.1:n.7578+118G=
XM_024454388.1:c.12504+118G=	XP_024310156.1:n.12504+118G=
XM_024454389.1:c.12093+118G=	XP_024310157.1:n.12093+118G=
NM_001369.3:c.13491+118G= MANE Select	NP_001360.1:n.13491+118G=