Canonical Allele Identifier: CA1528423473

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13753332T= , CM000667.2:g.13753332T=	GRCh38
NC_000005.9:g.13753441T= , CM000667.1:g.13753441T=	GRCh37
NC_000005.8:g.13806441T=	NCBI36
NG_013081.1:g.196149A=
NG_013081.2:g.196149A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.10773A= MANE Select	ENSP00000265104.4:p.Gly3591=
ENST00000681290.1:c.10728A=	ENSP00000505288.1:p.Gly3576=
ENST00000265104.4:c.10773A=	ENSP00000265104.4:p.Gly3591=
NM_001369.2:c.10773A=	NP_001360.1:p.Gly3591=
XM_005248262.2:c.10728A=	XP_005248319.1:p.Gly3576=
XM_005248262.3:c.10881A=	XP_005248319.2:p.Gly3627=
XM_017009177.1:c.10881A=	XP_016864666.1:p.Gly3627=
XM_017009178.1:c.9786A=	XP_016864667.1:p.Gly3262=
XM_017009179.2:c.9786A=	XP_016864668.1:p.Gly3262=
XM_017009180.1:c.10881A=	XP_016864669.1:p.Gly3627=
XM_017009181.1:c.10881A=	XP_016864670.1:p.Gly3627=
XM_017009182.1:c.10881A=	XP_016864671.1:p.Gly3627=
XM_017009185.1:c.5970A=	XP_016864674.1:p.Gly1990=
XM_017009186.1:c.5523A=	XP_016864675.1:p.Gly1841=
XM_017009188.1:c.4860A=	XP_016864677.1:p.Gly1620=
XM_024454388.1:c.9786A=	XP_024310156.1:p.Gly3262=
XM_024454389.1:c.9375A=	XP_024310157.1:p.Gly3125=
NM_001369.3:c.10773A= MANE Select	NP_001360.1:p.Gly3591=