Canonical Allele Identifier: CA1528441829

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13793942T= , CM000667.2:g.13793942T=	GRCh38
NC_000005.9:g.13794051T= , CM000667.1:g.13794051T=	GRCh37
NC_000005.8:g.13847051T=	NCBI36
NG_013081.1:g.155539A=
NG_013081.2:g.155539A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000265104.5:c.8004A= MANE Select	ENSP00000265104.4:p.Gly2668=
ENST00000681290.1:c.7959A=	ENSP00000505288.1:p.Gly2653=
ENST00000265104.4:c.8004A=	ENSP00000265104.4:p.Gly2668=
NM_001369.2:c.8004A=	NP_001360.1:p.Gly2668=
XM_005248262.2:c.7959A=	XP_005248319.1:p.Gly2653=
XM_011513990.1:c.8004A=	XP_011512292.1:p.Gly2668=
XR_925598.1:n.8211A=
XM_005248262.3:c.8112A=	XP_005248319.2:p.Gly2704=
XM_017009177.1:c.8112A=	XP_016864666.1:p.Gly2704=
XM_017009178.1:c.7017A=	XP_016864667.1:p.Gly2339=
XM_017009179.2:c.7017A=	XP_016864668.1:p.Gly2339=
XM_017009180.1:c.8112A=	XP_016864669.1:p.Gly2704=
XM_017009181.1:c.8112A=	XP_016864670.1:p.Gly2704=
XM_017009182.1:c.8112A=	XP_016864671.1:p.Gly2704=
XM_017009183.1:c.8112A=	XP_016864672.1:p.Gly2704=
XM_017009184.1:c.8112A=	XP_016864673.1:p.Gly2704=
XM_017009185.1:c.3201A=	XP_016864674.1:p.Gly1067=
XM_017009186.1:c.2754A=	XP_016864675.1:p.Gly918=
XM_017009188.1:c.2091A=	XP_016864677.1:p.Gly697=
XM_024454388.1:c.7017A=	XP_024310156.1:p.Gly2339=
XM_024454389.1:c.6606A=	XP_024310157.1:p.Gly2202=
XR_001742034.1:n.8129A=
XR_001742035.1:n.8129A=
NM_001369.3:c.8004A= MANE Select	NP_001360.1:p.Gly2668=