Canonical Allele Identifier: CA1528476464

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13870927T= , CM000667.2:g.13870927T=	GRCh38
NC_000005.9:g.13871036T= , CM000667.1:g.13871036T=	GRCh37
NC_000005.8:g.13924036T=	NCBI36
NG_013081.1:g.78554A=
NG_013081.2:g.78554A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.3674A= MANE Select	ENSP00000265104.4:p.Tyr1225=
ENST00000681290.1:c.3629A=	ENSP00000505288.1:p.Tyr1210=
ENST00000265104.4:c.3674A=	ENSP00000265104.4:p.Tyr1225=
NM_001369.2:c.3674A=	NP_001360.1:p.Tyr1225=
XM_005248262.2:c.3629A=	XP_005248319.1:p.Tyr1210=
XM_011513990.1:c.3674A=	XP_011512292.1:p.Tyr1225=
XR_925598.1:n.3881A=
XM_005248262.3:c.3782A=	XP_005248319.2:p.Tyr1261=
XM_017009177.1:c.3782A=	XP_016864666.1:p.Tyr1261=
XM_017009178.1:c.2687A=	XP_016864667.1:p.Tyr896=
XM_017009179.2:c.2687A=	XP_016864668.1:p.Tyr896=
XM_017009180.1:c.3782A=	XP_016864669.1:p.Tyr1261=
XM_017009181.1:c.3782A=	XP_016864670.1:p.Tyr1261=
XM_017009182.1:c.3782A=	XP_016864671.1:p.Tyr1261=
XM_017009183.1:c.3782A=	XP_016864672.1:p.Tyr1261=
XM_017009184.1:c.3782A=	XP_016864673.1:p.Tyr1261=
XM_017009187.1:c.3782A=	XP_016864676.1:p.Tyr1261=
XM_024454388.1:c.2687A=	XP_024310156.1:p.Tyr896=
XM_024454389.1:c.2276A=	XP_024310157.1:p.Tyr759=
XR_001742034.1:n.3799A=
XR_001742035.1:n.3799A=
NM_001369.3:c.3674A= MANE Select	NP_001360.1:p.Tyr1225=