Canonical Allele Identifier: CA1528431174

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13770765G= , CM000667.2:g.13770765G=	GRCh38
NC_000005.9:g.13770874G= , CM000667.1:g.13770874G=	GRCh37
NC_000005.8:g.13823874G=	NCBI36
NG_013081.1:g.178716C=
NG_013081.2:g.178716C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000265104.5:c.9589C= MANE Select	ENSP00000265104.4:p.Arg3197=
ENST00000681290.1:c.9544C=	ENSP00000505288.1:p.Arg3182=
ENST00000265104.4:c.9589C=	ENSP00000265104.4:p.Arg3197=
ENST00000504001.3:n.301C=
NM_001369.2:c.9589C=	NP_001360.1:p.Arg3197=
XM_005248262.2:c.9544C=	XP_005248319.1:p.Arg3182=
XM_005248262.3:c.9697C=	XP_005248319.2:p.Arg3233=
XM_017009177.1:c.9697C=	XP_016864666.1:p.Arg3233=
XM_017009178.1:c.8602C=	XP_016864667.1:p.Arg2868=
XM_017009179.2:c.8602C=	XP_016864668.1:p.Arg2868=
XM_017009180.1:c.9697C=	XP_016864669.1:p.Arg3233=
XM_017009181.1:c.9697C=	XP_016864670.1:p.Arg3233=
XM_017009182.1:c.9697C=	XP_016864671.1:p.Arg3233=
XM_017009183.1:c.9697C=	XP_016864672.1:p.Arg3233=
XM_017009185.1:c.4786C=	XP_016864674.1:p.Arg1596=
XM_017009186.1:c.4339C=	XP_016864675.1:p.Arg1447=
XM_017009188.1:c.3676C=	XP_016864677.1:p.Arg1226=
XM_024454388.1:c.8602C=	XP_024310156.1:p.Arg2868=
XM_024454389.1:c.8191C=	XP_024310157.1:p.Arg2731=
NM_001369.3:c.9589C= MANE Select	NP_001360.1:p.Arg3197=