Canonical Allele Identifier: CA443535679

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13776575G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13776466G>T , CM000667.2:g.13776466G>T	GRCh38
NC_000005.9:g.13776575G>T , CM000667.1:g.13776575G>T	GRCh37
NC_000005.8:g.13829575G>T	NCBI36
NG_013081.1:g.173015C>A
NG_013081.2:g.173015C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.9346C>A MANE Select	ENSP00000265104.4:p.Arg3116=
ENST00000681290.1:c.9301C>A	ENSP00000505288.1:p.Arg3101=
ENST00000265104.4:c.9346C>A	ENSP00000265104.4:p.Arg3116=
NM_001369.2:c.9346C>A	NP_001360.1:p.Arg3116=
XM_005248262.2:c.9301C>A	XP_005248319.1:p.Arg3101=
XM_005248262.3:c.9454C>A	XP_005248319.2:p.Arg3152=
XM_017009177.1:c.9454C>A	XP_016864666.1:p.Arg3152=
XM_017009178.1:c.8359C>A	XP_016864667.1:p.Arg2787=
XM_017009179.2:c.8359C>A	XP_016864668.1:p.Arg2787=
XM_017009180.1:c.9454C>A	XP_016864669.1:p.Arg3152=
XM_017009181.1:c.9454C>A	XP_016864670.1:p.Arg3152=
XM_017009182.1:c.9454C>A	XP_016864671.1:p.Arg3152=
XM_017009183.1:c.9454C>A	XP_016864672.1:p.Arg3152=
XM_017009185.1:c.4543C>A	XP_016864674.1:p.Arg1515=
XM_017009186.1:c.4096C>A	XP_016864675.1:p.Arg1366=
XM_017009188.1:c.3433C>A	XP_016864677.1:p.Arg1145=
XM_024454388.1:c.8359C>A	XP_024310156.1:p.Arg2787=
XM_024454389.1:c.7948C>A	XP_024310157.1:p.Arg2650=
NM_001369.3:c.9346C>A MANE Select	NP_001360.1:p.Arg3116=