Canonical Allele Identifier: CA1528415138

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13735926G= , CM000667.2:g.13735926G=	GRCh38
NC_000005.9:g.13736035G= , CM000667.1:g.13736035G=	GRCh37
NC_000005.8:g.13789035G=	NCBI36
NG_013081.1:g.213555C=
NG_013081.2:g.213555C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.11462C= MANE Select	ENSP00000265104.4:p.Thr3821=
ENST00000681290.1:c.11417C=	ENSP00000505288.1:p.Thr3806=
ENST00000265104.4:c.11462C=	ENSP00000265104.4:p.Thr3821=
NM_001369.2:c.11462C=	NP_001360.1:p.Thr3821=
XM_005248262.2:c.11417C=	XP_005248319.1:p.Thr3806=
XM_005248262.3:c.11570C=	XP_005248319.2:p.Thr3857=
XM_017009177.1:c.11570C=	XP_016864666.1:p.Thr3857=
XM_017009178.1:c.10475C=	XP_016864667.1:p.Thr3492=
XM_017009179.2:c.10475C=	XP_016864668.1:p.Thr3492=
XM_017009180.1:c.11570C=	XP_016864669.1:p.Thr3857=
XM_017009181.1:c.11570C=	XP_016864670.1:p.Thr3857=
XM_017009182.1:c.11326C=	XP_016864671.1:p.Arg3776=
XM_017009185.1:c.6659C=	XP_016864674.1:p.Thr2220=
XM_017009186.1:c.6212C=	XP_016864675.1:p.Thr2071=
XM_017009188.1:c.5549C=	XP_016864677.1:p.Thr1850=
XM_024454388.1:c.10475C=	XP_024310156.1:p.Thr3492=
XM_024454389.1:c.10064C=	XP_024310157.1:p.Thr3355=
NM_001369.3:c.11462C= MANE Select	NP_001360.1:p.Thr3821=