Canonical Allele Identifier: CA443536827

Gene: DNAH5

Linked Data

• ClinVar Variation Id: 2904139
• ClinVar RCV Id: RCV003651526
• gnomAD v4: 5-13901432-A-C
• MyVariant Identifiers: chr5:g.13901541A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13901432A>C , CM000667.2:g.13901432A>C	GRCh38
NC_000005.9:g.13901541A>C , CM000667.1:g.13901541A>C	GRCh37
NC_000005.8:g.13954541A>C	NCBI36
NG_013081.1:g.48049T>G
NG_013081.2:g.48049T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.1872T>G MANE Select	ENSP00000265104.4:p.Ala624=
ENST00000681290.1:c.1827T>G	ENSP00000505288.1:p.Ala609=
ENST00000265104.4:c.1872T>G	ENSP00000265104.4:p.Ala624=
NM_001369.2:c.1872T>G	NP_001360.1:p.Ala624=
XM_005248262.2:c.1827T>G	XP_005248319.1:p.Ala609=
XM_011513990.1:c.1872T>G	XP_011512292.1:p.Ala624=
XR_925598.1:n.2079T>G
XM_005248262.3:c.1980T>G	XP_005248319.2:p.Ala660=
XM_017009177.1:c.1980T>G	XP_016864666.1:p.Ala660=
XM_017009178.1:c.885T>G	XP_016864667.1:p.Ala295=
XM_017009179.2:c.885T>G	XP_016864668.1:p.Ala295=
XM_017009180.1:c.1980T>G	XP_016864669.1:p.Ala660=
XM_017009181.1:c.1980T>G	XP_016864670.1:p.Ala660=
XM_017009182.1:c.1980T>G	XP_016864671.1:p.Ala660=
XM_017009183.1:c.1980T>G	XP_016864672.1:p.Ala660=
XM_017009184.1:c.1980T>G	XP_016864673.1:p.Ala660=
XM_017009187.1:c.1980T>G	XP_016864676.1:p.Ala660=
XM_024454388.1:c.885T>G	XP_024310156.1:p.Ala295=
XM_024454389.1:c.474T>G	XP_024310157.1:p.Ala158=
XR_001742034.1:n.1997T>G
XR_001742035.1:n.1997T>G
NM_001369.3:c.1872T>G MANE Select	NP_001360.1:p.Ala624=