Canonical Allele Identifier: CA359211268

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13841866C>G (hg19) ; chr5:g.13841757C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13841757C>G , CM000667.2:g.13841757C>G	GRCh38
NC_000005.9:g.13841866C>G , CM000667.1:g.13841866C>G	GRCh37
NC_000005.8:g.13894866C>G	NCBI36
NG_013081.1:g.107724G>C
NG_013081.2:g.107724G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.5419G>C MANE Select	ENSP00000265104.4:p.Ala1807Pro
ENST00000681290.1:c.5374G>C	ENSP00000505288.1:p.Ala1792Pro
ENST00000265104.4:c.5419G>C	ENSP00000265104.4:p.Ala1807Pro
NM_001369.2:c.5419G>C	NP_001360.1:p.Ala1807Pro
XM_005248262.2:c.5374G>C	XP_005248319.1:p.Ala1792Pro
XM_011513990.1:c.5419G>C	XP_011512292.1:p.Ala1807Pro
XR_925598.1:n.5626G>C
XM_005248262.3:c.5527G>C	XP_005248319.2:p.Ala1843Pro
XM_017009177.1:c.5527G>C	XP_016864666.1:p.Ala1843Pro
XM_017009178.1:c.4432G>C	XP_016864667.1:p.Ala1478Pro
XM_017009179.2:c.4432G>C	XP_016864668.1:p.Ala1478Pro
XM_017009180.1:c.5527G>C	XP_016864669.1:p.Ala1843Pro
XM_017009181.1:c.5527G>C	XP_016864670.1:p.Ala1843Pro
XM_017009182.1:c.5527G>C	XP_016864671.1:p.Ala1843Pro
XM_017009183.1:c.5527G>C	XP_016864672.1:p.Ala1843Pro
XM_017009184.1:c.5527G>C	XP_016864673.1:p.Ala1843Pro
XM_017009185.1:c.616G>C	XP_016864674.1:p.Ala206Pro
XM_017009186.1:c.169G>C	XP_016864675.1:p.Ala57Pro
XM_017009187.1:c.5527G>C	XP_016864676.1:p.Ala1843Pro
XM_024454388.1:c.4432G>C	XP_024310156.1:p.Ala1478Pro
XM_024454389.1:c.4021G>C	XP_024310157.1:p.Ala1341Pro
XR_001742034.1:n.5544G>C
XR_001742035.1:n.5544G>C
NM_001369.3:c.5419G>C MANE Select	NP_001360.1:p.Ala1807Pro