Canonical Allele Identifier: CA1528479772
Gene: DNAH5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13876857_13876858delinsCA , CM000667.2:g.13876857_13876858delinsCA GRCh38
NC_000005.9:g.13876966_13876967delinsCA , CM000667.1:g.13876966_13876967delinsCA GRCh37
NC_000005.8:g.13929966_13929967delinsCA NCBI36
NG_013081.1:g.72623_72624delinsTG
NG_013081.2:g.72623_72624delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000265104.5:c.3263-41_3263-40delinsTG MANE Select ENSP00000265104.4:n.3263-41_3263-40delinsTG
ENST00000681290.1:c.3218-41_3218-40delinsTG ENSP00000505288.1:n.3218-41_3218-40delinsTG
ENST00000265104.4:c.3263-41_3263-40delinsTG ENSP00000265104.4:n.3263-41_3263-40delinsTG
NM_001369.2:c.3263-41_3263-40delinsTG NP_001360.1:n.3263-41_3263-40delinsTG
XM_005248262.2:c.3218-41_3218-40delinsTG XP_005248319.1:n.3218-41_3218-40delinsTG
XM_011513990.1:c.3263-41_3263-40delinsTG XP_011512292.1:n.3263-41_3263-40delinsTG
XR_925598.1:n.3470-41_3470-40delinsTG
XM_005248262.3:c.3371-41_3371-40delinsTG XP_005248319.2:n.3371-41_3371-40delinsTG
XM_017009177.1:c.3371-41_3371-40delinsTG XP_016864666.1:n.3371-41_3371-40delinsTG
XM_017009178.1:c.2276-41_2276-40delinsTG XP_016864667.1:n.2276-41_2276-40delinsTG
XM_017009179.2:c.2276-41_2276-40delinsTG XP_016864668.1:n.2276-41_2276-40delinsTG
XM_017009180.1:c.3371-41_3371-40delinsTG XP_016864669.1:n.3371-41_3371-40delinsTG
XM_017009181.1:c.3371-41_3371-40delinsTG XP_016864670.1:n.3371-41_3371-40delinsTG
XM_017009182.1:c.3371-41_3371-40delinsTG XP_016864671.1:n.3371-41_3371-40delinsTG
XM_017009183.1:c.3371-41_3371-40delinsTG XP_016864672.1:n.3371-41_3371-40delinsTG
XM_017009184.1:c.3371-41_3371-40delinsTG XP_016864673.1:n.3371-41_3371-40delinsTG
XM_017009187.1:c.3371-41_3371-40delinsTG XP_016864676.1:n.3371-41_3371-40delinsTG
XM_024454388.1:c.2276-41_2276-40delinsTG XP_024310156.1:n.2276-41_2276-40delinsTG
XM_024454389.1:c.1865-41_1865-40delinsTG XP_024310157.1:n.1865-41_1865-40delinsTG
XR_001742034.1:n.3388-41_3388-40delinsTG
XR_001742035.1:n.3388-41_3388-40delinsTG
NM_001369.3:c.3263-41_3263-40delinsTG MANE Select NP_001360.1:n.3263-41_3263-40delinsTG