Canonical Allele Identifier: CA1528403768

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13708222C= , CM000667.2:g.13708222C=	GRCh38
NC_000005.9:g.13708331C= , CM000667.1:g.13708331C=	GRCh37
NC_000005.8:g.13761331C=	NCBI36
NG_013081.1:g.241259G=
NG_013081.2:g.241259G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683611.1:n.572G=
ENST00000265104.5:c.13239G= MANE Select	ENSP00000265104.4:p.Glu4413=
ENST00000681290.1:c.13194G=	ENSP00000505288.1:p.Glu4398=
ENST00000265104.4:c.13239G=	ENSP00000265104.4:p.Glu4413=
NM_001369.2:c.13239G=	NP_001360.1:p.Glu4413=
XM_005248262.2:c.13194G=	XP_005248319.1:p.Glu4398=
XM_005248262.3:c.13347G=	XP_005248319.2:p.Glu4449=
XM_017009177.1:c.12927G=	XP_016864666.1:p.Glu4309=
XM_017009178.1:c.12252G=	XP_016864667.1:p.Glu4084=
XM_017009179.2:c.12252G=	XP_016864668.1:p.Glu4084=
XM_017009185.1:c.8436G=	XP_016864674.1:p.Glu2812=
XM_017009186.1:c.7989G=	XP_016864675.1:p.Glu2663=
XM_017009188.1:c.7326G=	XP_016864677.1:p.Glu2442=
XM_024454388.1:c.12252G=	XP_024310156.1:p.Glu4084=
XM_024454389.1:c.11841G=	XP_024310157.1:p.Glu3947=
NM_001369.3:c.13239G= MANE Select	NP_001360.1:p.Glu4413=