Canonical Allele Identifier: CA1528422952

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13752227C= , CM000667.2:g.13752227C=	GRCh38
NC_000005.9:g.13752336C= , CM000667.1:g.13752336C=	GRCh37
NC_000005.8:g.13805336C=	NCBI36
NG_013081.1:g.197254G=
NG_013081.2:g.197254G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.10935G= MANE Select	ENSP00000265104.4:p.Arg3645=
ENST00000681290.1:c.10890G=	ENSP00000505288.1:p.Arg3630=
ENST00000265104.4:c.10935G=	ENSP00000265104.4:p.Arg3645=
NM_001369.2:c.10935G=	NP_001360.1:p.Arg3645=
XM_005248262.2:c.10890G=	XP_005248319.1:p.Arg3630=
XM_005248262.3:c.11043G=	XP_005248319.2:p.Arg3681=
XM_017009177.1:c.11043G=	XP_016864666.1:p.Arg3681=
XM_017009178.1:c.9948G=	XP_016864667.1:p.Arg3316=
XM_017009179.2:c.9948G=	XP_016864668.1:p.Arg3316=
XM_017009180.1:c.11043G=	XP_016864669.1:p.Arg3681=
XM_017009181.1:c.11043G=	XP_016864670.1:p.Arg3681=
XM_017009182.1:c.11043G=	XP_016864671.1:p.Arg3681=
XM_017009185.1:c.6132G=	XP_016864674.1:p.Arg2044=
XM_017009186.1:c.5685G=	XP_016864675.1:p.Arg1895=
XM_017009188.1:c.5022G=	XP_016864677.1:p.Arg1674=
XM_024454388.1:c.9948G=	XP_024310156.1:p.Arg3316=
XM_024454389.1:c.9537G=	XP_024310157.1:p.Arg3179=
NM_001369.3:c.10935G= MANE Select	NP_001360.1:p.Arg3645=