Canonical Allele Identifier: CA3203671

Gene: DNAH5

Linked Data

• dbSNP Id: rs753056743
• ExAC: 5:13841834 T / C
• gnomAD v2: 5-13841834-T-C
• gnomAD v4: 5-13841725-T-C
• MyVariant Identifiers: chr5:g.13841834T>C (hg19) ; chr5:g.13841725T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13841725T>C , CM000667.2:g.13841725T>C	GRCh38
NC_000005.9:g.13841834T>C , CM000667.1:g.13841834T>C	GRCh37
NC_000005.8:g.13894834T>C	NCBI36
NG_013081.1:g.107756A>G
NG_013081.2:g.107756A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.5451A>G MANE Select	ENSP00000265104.4:p.Gln1817=
ENST00000681290.1:c.5406A>G	ENSP00000505288.1:p.Gln1802=
ENST00000265104.4:c.5451A>G	ENSP00000265104.4:p.Gln1817=
NM_001369.2:c.5451A>G	NP_001360.1:p.Gln1817=
XM_005248262.2:c.5406A>G	XP_005248319.1:p.Gln1802=
XM_011513990.1:c.5451A>G	XP_011512292.1:p.Gln1817=
XR_925598.1:n.5658A>G
XM_005248262.3:c.5559A>G	XP_005248319.2:p.Gln1853=
XM_017009177.1:c.5559A>G	XP_016864666.1:p.Gln1853=
XM_017009178.1:c.4464A>G	XP_016864667.1:p.Gln1488=
XM_017009179.2:c.4464A>G	XP_016864668.1:p.Gln1488=
XM_017009180.1:c.5559A>G	XP_016864669.1:p.Gln1853=
XM_017009181.1:c.5559A>G	XP_016864670.1:p.Gln1853=
XM_017009182.1:c.5559A>G	XP_016864671.1:p.Gln1853=
XM_017009183.1:c.5559A>G	XP_016864672.1:p.Gln1853=
XM_017009184.1:c.5559A>G	XP_016864673.1:p.Gln1853=
XM_017009185.1:c.648A>G	XP_016864674.1:p.Gln216=
XM_017009186.1:c.201A>G	XP_016864675.1:p.Gln67=
XM_017009187.1:c.5559A>G	XP_016864676.1:p.Gln1853=
XM_024454388.1:c.4464A>G	XP_024310156.1:p.Gln1488=
XM_024454389.1:c.4053A>G	XP_024310157.1:p.Gln1351=
XR_001742034.1:n.5576A>G
XR_001742035.1:n.5576A>G
NM_001369.3:c.5451A>G MANE Select	NP_001360.1:p.Gln1817=