Canonical Allele Identifier: CA16612017

Gene: DNAH5

Linked Data

• ClinVar Variation Id: 407216
• ClinVar RCV Id: RCV000465113
• dbSNP Id: rs759059925
• MyVariant Identifiers: chr5:g.13922317C>A (hg19) ; chr5:g.13922208C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13922208C>A , CM000667.2:g.13922208C>A	GRCh38
NC_000005.9:g.13922317C>A , CM000667.1:g.13922317C>A	GRCh37
NC_000005.8:g.13975317C>A	NCBI36
NG_013081.1:g.27273G>T
NG_013081.2:g.27273G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000680213.2:n.615G>T
ENST00000682376.1:n.603G>T
ENST00000682586.1:n.603G>T
ENST00000683011.1:n.498G>T
ENST00000683967.1:n.609G>T
ENST00000684013.1:n.609G>T
ENST00000684099.1:n.654G>T
ENST00000265104.5:c.559G>T MANE Select	ENSP00000265104.4:p.Glu187Ter
ENST00000680213.1:c.319G>T	ENSP00000506622.1:p.Glu107Ter
ENST00000681290.1:c.514G>T	ENSP00000505288.1:p.Glu172Ter
ENST00000265104.4:c.559G>T	ENSP00000265104.4:p.Glu187Ter
ENST00000508040.1:n.918G>T
NM_001369.2:c.559G>T	NP_001360.1:p.Glu187Ter
XM_005248262.2:c.514G>T	XP_005248319.1:p.Glu172Ter
XM_011513990.1:c.559G>T	XP_011512292.1:p.Glu187Ter
XR_925598.1:n.766G>T
XM_005248262.3:c.667G>T	XP_005248319.2:p.Glu223Ter
XM_017009177.1:c.667G>T	XP_016864666.1:p.Glu223Ter
XM_017009178.1:c.-478G>T	XP_016864667.1:n.-478G>T
XM_017009180.1:c.667G>T	XP_016864669.1:p.Glu223Ter
XM_017009181.1:c.667G>T	XP_016864670.1:p.Glu223Ter
XM_017009182.1:c.667G>T	XP_016864671.1:p.Glu223Ter
XM_017009183.1:c.667G>T	XP_016864672.1:p.Glu223Ter
XM_017009184.1:c.667G>T	XP_016864673.1:p.Glu223Ter
XM_017009187.1:c.667G>T	XP_016864676.1:p.Glu223Ter
XM_024454388.1:c.-2348G>T	XP_024310156.1:n.-2348G>T
XM_024454389.1:c.-1401G>T	XP_024310157.1:n.-1401G>T
XR_001742034.1:n.684G>T
XR_001742035.1:n.684G>T
NM_001369.3:c.559G>T MANE Select	NP_001360.1:p.Glu187Ter