Canonical Allele Identifier: CA1528441642

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13793564A= , CM000667.2:g.13793564A=	GRCh38
NC_000005.9:g.13793673A= , CM000667.1:g.13793673A=	GRCh37
NC_000005.8:g.13846673A=	NCBI36
NG_013081.1:g.155917T=
NG_013081.2:g.155917T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.8175T= MANE Select	ENSP00000265104.4:p.Ser2725=
ENST00000681290.1:c.8130T=	ENSP00000505288.1:p.Ser2710=
ENST00000265104.4:c.8175T=	ENSP00000265104.4:p.Ser2725=
NM_001369.2:c.8175T=	NP_001360.1:p.Ser2725=
XM_005248262.2:c.8130T=	XP_005248319.1:p.Ser2710=
XM_011513990.1:c.8175T=	XP_011512292.1:p.Ser2725=
XR_925598.1:n.8382T=
XM_005248262.3:c.8283T=	XP_005248319.2:p.Ser2761=
XM_017009177.1:c.8283T=	XP_016864666.1:p.Ser2761=
XM_017009178.1:c.7188T=	XP_016864667.1:p.Ser2396=
XM_017009179.2:c.7188T=	XP_016864668.1:p.Ser2396=
XM_017009180.1:c.8283T=	XP_016864669.1:p.Ser2761=
XM_017009181.1:c.8283T=	XP_016864670.1:p.Ser2761=
XM_017009182.1:c.8283T=	XP_016864671.1:p.Ser2761=
XM_017009183.1:c.8283T=	XP_016864672.1:p.Ser2761=
XM_017009184.1:c.8283T=	XP_016864673.1:p.Ser2761=
XM_017009185.1:c.3372T=	XP_016864674.1:p.Ser1124=
XM_017009186.1:c.2925T=	XP_016864675.1:p.Ser975=
XM_017009188.1:c.2262T=	XP_016864677.1:p.Ser754=
XM_024454388.1:c.7188T=	XP_024310156.1:p.Ser2396=
XM_024454389.1:c.6777T=	XP_024310157.1:p.Ser2259=
XR_001742034.1:n.8300T=
XR_001742035.1:n.8300T=
NM_001369.3:c.8175T= MANE Select	NP_001360.1:p.Ser2725=