Canonical Allele Identifier: CA359211468

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13841884G>T (hg19) ; chr5:g.13841775G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13841775G>T , CM000667.2:g.13841775G>T	GRCh38
NC_000005.9:g.13841884G>T , CM000667.1:g.13841884G>T	GRCh37
NC_000005.8:g.13894884G>T	NCBI36
NG_013081.1:g.107706C>A
NG_013081.2:g.107706C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000265104.5:c.5401C>A MANE Select	ENSP00000265104.4:p.His1801Asn
ENST00000681290.1:c.5356C>A	ENSP00000505288.1:p.His1786Asn
ENST00000265104.4:c.5401C>A	ENSP00000265104.4:p.His1801Asn
NM_001369.2:c.5401C>A	NP_001360.1:p.His1801Asn
XM_005248262.2:c.5356C>A	XP_005248319.1:p.His1786Asn
XM_011513990.1:c.5401C>A	XP_011512292.1:p.His1801Asn
XR_925598.1:n.5608C>A
XM_005248262.3:c.5509C>A	XP_005248319.2:p.His1837Asn
XM_017009177.1:c.5509C>A	XP_016864666.1:p.His1837Asn
XM_017009178.1:c.4414C>A	XP_016864667.1:p.His1472Asn
XM_017009179.2:c.4414C>A	XP_016864668.1:p.His1472Asn
XM_017009180.1:c.5509C>A	XP_016864669.1:p.His1837Asn
XM_017009181.1:c.5509C>A	XP_016864670.1:p.His1837Asn
XM_017009182.1:c.5509C>A	XP_016864671.1:p.His1837Asn
XM_017009183.1:c.5509C>A	XP_016864672.1:p.His1837Asn
XM_017009184.1:c.5509C>A	XP_016864673.1:p.His1837Asn
XM_017009185.1:c.598C>A	XP_016864674.1:p.His200Asn
XM_017009186.1:c.151C>A	XP_016864675.1:p.His51Asn
XM_017009187.1:c.5509C>A	XP_016864676.1:p.His1837Asn
XM_024454388.1:c.4414C>A	XP_024310156.1:p.His1472Asn
XM_024454389.1:c.4003C>A	XP_024310157.1:p.His1335Asn
XR_001742034.1:n.5526C>A
XR_001742035.1:n.5526C>A
NM_001369.3:c.5401C>A MANE Select	NP_001360.1:p.His1801Asn