Canonical Allele Identifier: CA1528435863

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13780874G= , CM000667.2:g.13780874G=	GRCh38
NC_000005.9:g.13780983G= , CM000667.1:g.13780983G=	GRCh37
NC_000005.8:g.13833983G=	NCBI36
NG_013081.1:g.168607C=
NG_013081.2:g.168607C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.8906C= MANE Select	ENSP00000265104.4:p.Ala2969=
ENST00000681290.1:c.8861C=	ENSP00000505288.1:p.Ala2954=
ENST00000265104.4:c.8906C=	ENSP00000265104.4:p.Ala2969=
NM_001369.2:c.8906C=	NP_001360.1:p.Ala2969=
XM_005248262.2:c.8861C=	XP_005248319.1:p.Ala2954=
XM_011513990.1:c.8906C=	XP_011512292.1:p.Ala2969=
XR_925598.1:n.9028-3519C=
XM_005248262.3:c.9014C=	XP_005248319.2:p.Ala3005=
XM_017009177.1:c.9014C=	XP_016864666.1:p.Ala3005=
XM_017009178.1:c.7919C=	XP_016864667.1:p.Ala2640=
XM_017009179.2:c.7919C=	XP_016864668.1:p.Ala2640=
XM_017009180.1:c.9014C=	XP_016864669.1:p.Ala3005=
XM_017009181.1:c.9014C=	XP_016864670.1:p.Ala3005=
XM_017009182.1:c.9014C=	XP_016864671.1:p.Ala3005=
XM_017009183.1:c.9014C=	XP_016864672.1:p.Ala3005=
XM_017009184.1:c.9014C=	XP_016864673.1:p.Ala3005=
XM_017009185.1:c.4103C=	XP_016864674.1:p.Ala1368=
XM_017009186.1:c.3656C=	XP_016864675.1:p.Ala1219=
XM_017009188.1:c.2993C=	XP_016864677.1:p.Ala998=
XM_024454388.1:c.7919C=	XP_024310156.1:p.Ala2640=
XM_024454389.1:c.7508C=	XP_024310157.1:p.Ala2503=
XR_001742034.1:n.8946-3519C=
XR_001742035.1:n.8946-3519C=
NM_001369.3:c.8906C= MANE Select	NP_001360.1:p.Ala2969=