Canonical Allele Identifier: CA443535815

Gene: DNAH5

Linked Data

• COSMIC: COSM735545
• MyVariant Identifiers: chr5:g.13776797G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13776688G>T , CM000667.2:g.13776688G>T	GRCh38
NC_000005.9:g.13776797G>T , CM000667.1:g.13776797G>T	GRCh37
NC_000005.8:g.13829797G>T	NCBI36
NG_013081.1:g.172793C>A
NG_013081.2:g.172793C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.9124C>A MANE Select	ENSP00000265104.4:p.Arg3042=
ENST00000681290.1:c.9079C>A	ENSP00000505288.1:p.Arg3027=
ENST00000265104.4:c.9124C>A	ENSP00000265104.4:p.Arg3042=
NM_001369.2:c.9124C>A	NP_001360.1:p.Arg3042=
XM_005248262.2:c.9079C>A	XP_005248319.1:p.Arg3027=
XM_011513990.1:c.*11C>A	XP_011512292.1:n.*11C>A
XR_925598.1:n.9195C>A
XM_005248262.3:c.9232C>A	XP_005248319.2:p.Arg3078=
XM_017009177.1:c.9232C>A	XP_016864666.1:p.Arg3078=
XM_017009178.1:c.8137C>A	XP_016864667.1:p.Arg2713=
XM_017009179.2:c.8137C>A	XP_016864668.1:p.Arg2713=
XM_017009180.1:c.9232C>A	XP_016864669.1:p.Arg3078=
XM_017009181.1:c.9232C>A	XP_016864670.1:p.Arg3078=
XM_017009182.1:c.9232C>A	XP_016864671.1:p.Arg3078=
XM_017009183.1:c.9232C>A	XP_016864672.1:p.Arg3078=
XM_017009184.1:c.*11C>A	XP_016864673.1:n.*11C>A
XM_017009185.1:c.4321C>A	XP_016864674.1:p.Arg1441=
XM_017009186.1:c.3874C>A	XP_016864675.1:p.Arg1292=
XM_017009188.1:c.3211C>A	XP_016864677.1:p.Arg1071=
XM_024454388.1:c.8137C>A	XP_024310156.1:p.Arg2713=
XM_024454389.1:c.7726C>A	XP_024310157.1:p.Arg2576=
XR_001742034.1:n.9118C>A
XR_001742035.1:n.9113C>A
NM_001369.3:c.9124C>A MANE Select	NP_001360.1:p.Arg3042=