Canonical Allele Identifier: CA1528435859

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13780865A= , CM000667.2:g.13780865A=	GRCh38
NC_000005.9:g.13780974A= , CM000667.1:g.13780974A=	GRCh37
NC_000005.8:g.13833974A=	NCBI36
NG_013081.1:g.168616T=
NG_013081.2:g.168616T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000265104.5:c.8915T= MANE Select	ENSP00000265104.4:p.Ile2972=
ENST00000681290.1:c.8870T=	ENSP00000505288.1:p.Ile2957=
ENST00000265104.4:c.8915T=	ENSP00000265104.4:p.Ile2972=
NM_001369.2:c.8915T=	NP_001360.1:p.Ile2972=
XM_005248262.2:c.8870T=	XP_005248319.1:p.Ile2957=
XM_011513990.1:c.8915T=	XP_011512292.1:p.Ile2972=
XR_925598.1:n.9028-3510T=
XM_005248262.3:c.9023T=	XP_005248319.2:p.Ile3008=
XM_017009177.1:c.9023T=	XP_016864666.1:p.Ile3008=
XM_017009178.1:c.7928T=	XP_016864667.1:p.Ile2643=
XM_017009179.2:c.7928T=	XP_016864668.1:p.Ile2643=
XM_017009180.1:c.9023T=	XP_016864669.1:p.Ile3008=
XM_017009181.1:c.9023T=	XP_016864670.1:p.Ile3008=
XM_017009182.1:c.9023T=	XP_016864671.1:p.Ile3008=
XM_017009183.1:c.9023T=	XP_016864672.1:p.Ile3008=
XM_017009184.1:c.9023T=	XP_016864673.1:p.Ile3008=
XM_017009185.1:c.4112T=	XP_016864674.1:p.Ile1371=
XM_017009186.1:c.3665T=	XP_016864675.1:p.Ile1222=
XM_017009188.1:c.3002T=	XP_016864677.1:p.Ile1001=
XM_024454388.1:c.7928T=	XP_024310156.1:p.Ile2643=
XM_024454389.1:c.7517T=	XP_024310157.1:p.Ile2506=
XR_001742034.1:n.8946-3510T=
XR_001742035.1:n.8946-3510T=
NM_001369.3:c.8915T= MANE Select	NP_001360.1:p.Ile2972=