Canonical Allele Identifier: CA443536728

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13901445G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13901336G>A , CM000667.2:g.13901336G>A	GRCh38
NC_000005.9:g.13901445G>A , CM000667.1:g.13901445G>A	GRCh37
NC_000005.8:g.13954445G>A	NCBI36
NG_013081.1:g.48145C>T
NG_013081.2:g.48145C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.1968C>T MANE Select	ENSP00000265104.4:p.Ala656=
ENST00000681290.1:c.1923C>T	ENSP00000505288.1:p.Ala641=
ENST00000265104.4:c.1968C>T	ENSP00000265104.4:p.Ala656=
NM_001369.2:c.1968C>T	NP_001360.1:p.Ala656=
XM_005248262.2:c.1923C>T	XP_005248319.1:p.Ala641=
XM_011513990.1:c.1968C>T	XP_011512292.1:p.Ala656=
XR_925598.1:n.2175C>T
XM_005248262.3:c.2076C>T	XP_005248319.2:p.Ala692=
XM_017009177.1:c.2076C>T	XP_016864666.1:p.Ala692=
XM_017009178.1:c.981C>T	XP_016864667.1:p.Ala327=
XM_017009179.2:c.981C>T	XP_016864668.1:p.Ala327=
XM_017009180.1:c.2076C>T	XP_016864669.1:p.Ala692=
XM_017009181.1:c.2076C>T	XP_016864670.1:p.Ala692=
XM_017009182.1:c.2076C>T	XP_016864671.1:p.Ala692=
XM_017009183.1:c.2076C>T	XP_016864672.1:p.Ala692=
XM_017009184.1:c.2076C>T	XP_016864673.1:p.Ala692=
XM_017009187.1:c.2076C>T	XP_016864676.1:p.Ala692=
XM_024454388.1:c.981C>T	XP_024310156.1:p.Ala327=
XM_024454389.1:c.570C>T	XP_024310157.1:p.Ala190=
XR_001742034.1:n.2093C>T
XR_001742035.1:n.2093C>T
NM_001369.3:c.1968C>T MANE Select	NP_001360.1:p.Ala656=