Canonical Allele Identifier: CA1528463575
Gene: DNAH5 HGNC NCBI

Linked Data

dbSNP Id: rs1765246702

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13841962_13841963insAAAAAAAAA , CM000667.2:g.13841962_13841963insAAAAAAAAA GRCh38
NC_000005.9:g.13842071_13842072insAAAAAAAAA , CM000667.1:g.13842071_13842072insAAAAAAAAA GRCh37
NC_000005.8:g.13895071_13895072insAAAAAAAAA NCBI36
NG_013081.1:g.107523_107524insTTTTTTTTT
NG_013081.2:g.107523_107524insTTTTTTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000265104.5:c.5272-54_5272-53insTTTTTTTTT MANE Select ENSP00000265104.4:n.5272-54_5272-53insTTTTTTTTT
ENST00000681290.1:c.5227-54_5227-53insTTTTTTTTT ENSP00000505288.1:n.5227-54_5227-53insTTTTTTTTT
ENST00000265104.4:c.5272-54_5272-53insTTTTTTTTT ENSP00000265104.4:n.5272-54_5272-53insTTTTTTTTT
NM_001369.2:c.5272-54_5272-53insTTTTTTTTT NP_001360.1:n.5272-54_5272-53insTTTTTTTTT
XM_005248262.2:c.5227-54_5227-53insTTTTTTTTT XP_005248319.1:n.5227-54_5227-53insTTTTTTTTT
XM_011513990.1:c.5272-54_5272-53insTTTTTTTTT XP_011512292.1:n.5272-54_5272-53insTTTTTTTTT
XR_925598.1:n.5479-54_5479-53insTTTTTTTTT
XM_005248262.3:c.5380-54_5380-53insTTTTTTTTT XP_005248319.2:n.5380-54_5380-53insTTTTTTTTT
XM_017009177.1:c.5380-54_5380-53insTTTTTTTTT XP_016864666.1:n.5380-54_5380-53insTTTTTTTTT
XM_017009178.1:c.4285-54_4285-53insTTTTTTTTT XP_016864667.1:n.4285-54_4285-53insTTTTTTTTT
XM_017009179.2:c.4285-54_4285-53insTTTTTTTTT XP_016864668.1:n.4285-54_4285-53insTTTTTTTTT
XM_017009180.1:c.5380-54_5380-53insTTTTTTTTT XP_016864669.1:n.5380-54_5380-53insTTTTTTTTT
XM_017009181.1:c.5380-54_5380-53insTTTTTTTTT XP_016864670.1:n.5380-54_5380-53insTTTTTTTTT
XM_017009182.1:c.5380-54_5380-53insTTTTTTTTT XP_016864671.1:n.5380-54_5380-53insTTTTTTTTT
XM_017009183.1:c.5380-54_5380-53insTTTTTTTTT XP_016864672.1:n.5380-54_5380-53insTTTTTTTTT
XM_017009184.1:c.5380-54_5380-53insTTTTTTTTT XP_016864673.1:n.5380-54_5380-53insTTTTTTTTT
XM_017009185.1:c.469-54_469-53insTTTTTTTTT XP_016864674.1:n.469-54_469-53insTTTTTTTTT
XM_017009186.1:c.22-54_22-53insTTTTTTTTT XP_016864675.1:n.22-54_22-53insTTTTTTTTT
XM_017009187.1:c.5380-54_5380-53insTTTTTTTTT XP_016864676.1:n.5380-54_5380-53insTTTTTTTTT
XM_024454388.1:c.4285-54_4285-53insTTTTTTTTT XP_024310156.1:n.4285-54_4285-53insTTTTTTTTT
XM_024454389.1:c.3874-54_3874-53insTTTTTTTTT XP_024310157.1:n.3874-54_3874-53insTTTTTTTTT
XR_001742034.1:n.5397-54_5397-53insTTTTTTTTT
XR_001742035.1:n.5397-54_5397-53insTTTTTTTTT
NM_001369.3:c.5272-54_5272-53insTTTTTTTTT MANE Select NP_001360.1:n.5272-54_5272-53insTTTTTTTTT