Canonical Allele Identifier: CA443267344

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13794066T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13793957T>A , CM000667.2:g.13793957T>A	GRCh38
NC_000005.9:g.13794066T>A , CM000667.1:g.13794066T>A	GRCh37
NC_000005.8:g.13847066T>A	NCBI36
NG_013081.1:g.155524A>T
NG_013081.2:g.155524A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.7989A>T MANE Select	ENSP00000265104.4:p.Ile2663=
ENST00000681290.1:c.7944A>T	ENSP00000505288.1:p.Ile2648=
ENST00000265104.4:c.7989A>T	ENSP00000265104.4:p.Ile2663=
NM_001369.2:c.7989A>T	NP_001360.1:p.Ile2663=
XM_005248262.2:c.7944A>T	XP_005248319.1:p.Ile2648=
XM_011513990.1:c.7989A>T	XP_011512292.1:p.Ile2663=
XR_925598.1:n.8196A>T
XM_005248262.3:c.8097A>T	XP_005248319.2:p.Ile2699=
XM_017009177.1:c.8097A>T	XP_016864666.1:p.Ile2699=
XM_017009178.1:c.7002A>T	XP_016864667.1:p.Ile2334=
XM_017009179.2:c.7002A>T	XP_016864668.1:p.Ile2334=
XM_017009180.1:c.8097A>T	XP_016864669.1:p.Ile2699=
XM_017009181.1:c.8097A>T	XP_016864670.1:p.Ile2699=
XM_017009182.1:c.8097A>T	XP_016864671.1:p.Ile2699=
XM_017009183.1:c.8097A>T	XP_016864672.1:p.Ile2699=
XM_017009184.1:c.8097A>T	XP_016864673.1:p.Ile2699=
XM_017009185.1:c.3186A>T	XP_016864674.1:p.Ile1062=
XM_017009186.1:c.2739A>T	XP_016864675.1:p.Ile913=
XM_017009188.1:c.2076A>T	XP_016864677.1:p.Ile692=
XM_024454388.1:c.7002A>T	XP_024310156.1:p.Ile2334=
XM_024454389.1:c.6591A>T	XP_024310157.1:p.Ile2197=
XR_001742034.1:n.8114A>T
XR_001742035.1:n.8114A>T
NM_001369.3:c.7989A>T MANE Select	NP_001360.1:p.Ile2663=