Canonical Allele Identifier: CA1528441879

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13794055T= , CM000667.2:g.13794055T=	GRCh38
NC_000005.9:g.13794164T= , CM000667.1:g.13794164T=	GRCh37
NC_000005.8:g.13847164T=	NCBI36
NG_013081.1:g.155426A=
NG_013081.2:g.155426A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000265104.5:c.7891A= MANE Select	ENSP00000265104.4:p.Thr2631=
ENST00000681290.1:c.7846A=	ENSP00000505288.1:p.Thr2616=
ENST00000265104.4:c.7891A=	ENSP00000265104.4:p.Thr2631=
NM_001369.2:c.7891A=	NP_001360.1:p.Thr2631=
XM_005248262.2:c.7846A=	XP_005248319.1:p.Thr2616=
XM_011513990.1:c.7891A=	XP_011512292.1:p.Thr2631=
XR_925598.1:n.8098A=
XM_005248262.3:c.7999A=	XP_005248319.2:p.Thr2667=
XM_017009177.1:c.7999A=	XP_016864666.1:p.Thr2667=
XM_017009178.1:c.6904A=	XP_016864667.1:p.Thr2302=
XM_017009179.2:c.6904A=	XP_016864668.1:p.Thr2302=
XM_017009180.1:c.7999A=	XP_016864669.1:p.Thr2667=
XM_017009181.1:c.7999A=	XP_016864670.1:p.Thr2667=
XM_017009182.1:c.7999A=	XP_016864671.1:p.Thr2667=
XM_017009183.1:c.7999A=	XP_016864672.1:p.Thr2667=
XM_017009184.1:c.7999A=	XP_016864673.1:p.Thr2667=
XM_017009185.1:c.3088A=	XP_016864674.1:p.Thr1030=
XM_017009186.1:c.2641A=	XP_016864675.1:p.Thr881=
XM_017009187.1:c.8034A=	XP_016864676.1:p.Gly2678=
XM_017009188.1:c.1978A=	XP_016864677.1:p.Thr660=
XM_024454388.1:c.6904A=	XP_024310156.1:p.Thr2302=
XM_024454389.1:c.6493A=	XP_024310157.1:p.Thr2165=
XR_001742034.1:n.8016A=
XR_001742035.1:n.8016A=
NM_001369.3:c.7891A= MANE Select	NP_001360.1:p.Thr2631=