Canonical Allele Identifier: CA1528415137

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13735925C= , CM000667.2:g.13735925C=	GRCh38
NC_000005.9:g.13736034C= , CM000667.1:g.13736034C=	GRCh37
NC_000005.8:g.13789034C=	NCBI36
NG_013081.1:g.213556G=
NG_013081.2:g.213556G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.11463G= MANE Select	ENSP00000265104.4:p.Thr3821=
ENST00000681290.1:c.11418G=	ENSP00000505288.1:p.Thr3806=
ENST00000265104.4:c.11463G=	ENSP00000265104.4:p.Thr3821=
NM_001369.2:c.11463G=	NP_001360.1:p.Thr3821=
XM_005248262.2:c.11418G=	XP_005248319.1:p.Thr3806=
XM_005248262.3:c.11571G=	XP_005248319.2:p.Thr3857=
XM_017009177.1:c.11571G=	XP_016864666.1:p.Thr3857=
XM_017009178.1:c.10476G=	XP_016864667.1:p.Thr3492=
XM_017009179.2:c.10476G=	XP_016864668.1:p.Thr3492=
XM_017009180.1:c.11571G=	XP_016864669.1:p.Thr3857=
XM_017009181.1:c.11571G=	XP_016864670.1:p.Thr3857=
XM_017009182.1:c.11327G=	XP_016864671.1:p.Arg3776=
XM_017009185.1:c.6660G=	XP_016864674.1:p.Thr2220=
XM_017009186.1:c.6213G=	XP_016864675.1:p.Thr2071=
XM_017009188.1:c.5550G=	XP_016864677.1:p.Thr1850=
XM_024454388.1:c.10476G=	XP_024310156.1:p.Thr3492=
XM_024454389.1:c.10065G=	XP_024310157.1:p.Thr3355=
NM_001369.3:c.11463G= MANE Select	NP_001360.1:p.Thr3821=