Canonical Allele Identifier: CA175799
Gene: DNAH5 HGNC NCBI

Linked Data

ClinVar Variation Id: 163153
dbSNP Id: rs61747516
gnomAD v2: 5-13876888-C-T
gnomAD v3: 5-13876779-C-T
gnomAD v4: 5-13876779-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13876779C>T , CM000667.2:g.13876779C>T GRCh38
NC_000005.9:g.13876888C>T , CM000667.1:g.13876888C>T GRCh37
NC_000005.8:g.13929888C>T NCBI36
NG_013081.1:g.72702G>A
NG_013081.2:g.72702G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000265104.5:c.3301G>A MANE Select ENSP00000265104.4:p.Val1101Met
ENST00000681290.1:c.3256G>A ENSP00000505288.1:p.Val1086Met
ENST00000265104.4:c.3301G>A ENSP00000265104.4:p.Val1101Met
NM_001369.2:c.3301G>A NP_001360.1:p.Val1101Met
XM_005248262.2:c.3256G>A XP_005248319.1:p.Val1086Met
XM_011513990.1:c.3301G>A XP_011512292.1:p.Val1101Met
XR_925598.1:n.3508G>A
XM_005248262.3:c.3409G>A XP_005248319.2:p.Val1137Met
XM_017009177.1:c.3409G>A XP_016864666.1:p.Val1137Met
XM_017009178.1:c.2314G>A XP_016864667.1:p.Val772Met
XM_017009179.2:c.2314G>A XP_016864668.1:p.Val772Met
XM_017009180.1:c.3409G>A XP_016864669.1:p.Val1137Met
XM_017009181.1:c.3409G>A XP_016864670.1:p.Val1137Met
XM_017009182.1:c.3409G>A XP_016864671.1:p.Val1137Met
XM_017009183.1:c.3409G>A XP_016864672.1:p.Val1137Met
XM_017009184.1:c.3409G>A XP_016864673.1:p.Val1137Met
XM_017009187.1:c.3409G>A XP_016864676.1:p.Val1137Met
XM_024454388.1:c.2314G>A XP_024310156.1:p.Val772Met
XM_024454389.1:c.1903G>A XP_024310157.1:p.Val635Met
XR_001742034.1:n.3426G>A
XR_001742035.1:n.3426G>A
NM_001369.3:c.3301G>A MANE Select NP_001360.1:p.Val1101Met