Canonical Allele Identifier: CA443266077

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13793712T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13793603T>C , CM000667.2:g.13793603T>C	GRCh38
NC_000005.9:g.13793712T>C , CM000667.1:g.13793712T>C	GRCh37
NC_000005.8:g.13846712T>C	NCBI36
NG_013081.1:g.155878A>G
NG_013081.2:g.155878A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.8136A>G MANE Select	ENSP00000265104.4:p.Gly2712=
ENST00000681290.1:c.8091A>G	ENSP00000505288.1:p.Gly2697=
ENST00000265104.4:c.8136A>G	ENSP00000265104.4:p.Gly2712=
NM_001369.2:c.8136A>G	NP_001360.1:p.Gly2712=
XM_005248262.2:c.8091A>G	XP_005248319.1:p.Gly2697=
XM_011513990.1:c.8136A>G	XP_011512292.1:p.Gly2712=
XR_925598.1:n.8343A>G
XM_005248262.3:c.8244A>G	XP_005248319.2:p.Gly2748=
XM_017009177.1:c.8244A>G	XP_016864666.1:p.Gly2748=
XM_017009178.1:c.7149A>G	XP_016864667.1:p.Gly2383=
XM_017009179.2:c.7149A>G	XP_016864668.1:p.Gly2383=
XM_017009180.1:c.8244A>G	XP_016864669.1:p.Gly2748=
XM_017009181.1:c.8244A>G	XP_016864670.1:p.Gly2748=
XM_017009182.1:c.8244A>G	XP_016864671.1:p.Gly2748=
XM_017009183.1:c.8244A>G	XP_016864672.1:p.Gly2748=
XM_017009184.1:c.8244A>G	XP_016864673.1:p.Gly2748=
XM_017009185.1:c.3333A>G	XP_016864674.1:p.Gly1111=
XM_017009186.1:c.2886A>G	XP_016864675.1:p.Gly962=
XM_017009188.1:c.2223A>G	XP_016864677.1:p.Gly741=
XM_024454388.1:c.7149A>G	XP_024310156.1:p.Gly2383=
XM_024454389.1:c.6738A>G	XP_024310157.1:p.Gly2246=
XR_001742034.1:n.8261A>G
XR_001742035.1:n.8261A>G
NM_001369.3:c.8136A>G MANE Select	NP_001360.1:p.Gly2712=