Canonical Allele Identifier: CA443535399

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13871110A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13871001A>C , CM000667.2:g.13871001A>C	GRCh38
NC_000005.9:g.13871110A>C , CM000667.1:g.13871110A>C	GRCh37
NC_000005.8:g.13924110A>C	NCBI36
NG_013081.1:g.78480T>G
NG_013081.2:g.78480T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.3600T>G MANE Select	ENSP00000265104.4:p.Ala1200=
ENST00000681290.1:c.3555T>G	ENSP00000505288.1:p.Ala1185=
ENST00000265104.4:c.3600T>G	ENSP00000265104.4:p.Ala1200=
NM_001369.2:c.3600T>G	NP_001360.1:p.Ala1200=
XM_005248262.2:c.3555T>G	XP_005248319.1:p.Ala1185=
XM_011513990.1:c.3600T>G	XP_011512292.1:p.Ala1200=
XR_925598.1:n.3807T>G
XM_005248262.3:c.3708T>G	XP_005248319.2:p.Ala1236=
XM_017009177.1:c.3708T>G	XP_016864666.1:p.Ala1236=
XM_017009178.1:c.2613T>G	XP_016864667.1:p.Ala871=
XM_017009179.2:c.2613T>G	XP_016864668.1:p.Ala871=
XM_017009180.1:c.3708T>G	XP_016864669.1:p.Ala1236=
XM_017009181.1:c.3708T>G	XP_016864670.1:p.Ala1236=
XM_017009182.1:c.3708T>G	XP_016864671.1:p.Ala1236=
XM_017009183.1:c.3708T>G	XP_016864672.1:p.Ala1236=
XM_017009184.1:c.3708T>G	XP_016864673.1:p.Ala1236=
XM_017009187.1:c.3708T>G	XP_016864676.1:p.Ala1236=
XM_024454388.1:c.2613T>G	XP_024310156.1:p.Ala871=
XM_024454389.1:c.2202T>G	XP_024310157.1:p.Ala734=
XR_001742034.1:n.3725T>G
XR_001742035.1:n.3725T>G
NM_001369.3:c.3600T>G MANE Select	NP_001360.1:p.Ala1200=