Canonical Allele Identifier: CA2673274341
Gene: DNAH5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13841912_13841913insAAA , CM000667.2:g.13841912_13841913insAAA GRCh38
NC_000005.9:g.13842021_13842022insAAA , CM000667.1:g.13842021_13842022insAAA GRCh37
NC_000005.8:g.13895021_13895022insAAA NCBI36
NG_013081.1:g.107569_107570insTTT
NG_013081.2:g.107569_107570insTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000265104.5:c.5272-8_5272-7insTTT MANE Select ENSP00000265104.4:n.5272-8_5272-7insTTT
ENST00000681290.1:c.5227-8_5227-7insTTT ENSP00000505288.1:n.5227-8_5227-7insTTT
ENST00000265104.4:c.5272-8_5272-7insTTT ENSP00000265104.4:n.5272-8_5272-7insTTT
NM_001369.2:c.5272-8_5272-7insTTT NP_001360.1:n.5272-8_5272-7insTTT
XM_005248262.2:c.5227-8_5227-7insTTT XP_005248319.1:n.5227-8_5227-7insTTT
XM_011513990.1:c.5272-8_5272-7insTTT XP_011512292.1:n.5272-8_5272-7insTTT
XR_925598.1:n.5479-8_5479-7insTTT
XM_005248262.3:c.5380-8_5380-7insTTT XP_005248319.2:n.5380-8_5380-7insTTT
XM_017009177.1:c.5380-8_5380-7insTTT XP_016864666.1:n.5380-8_5380-7insTTT
XM_017009178.1:c.4285-8_4285-7insTTT XP_016864667.1:n.4285-8_4285-7insTTT
XM_017009179.2:c.4285-8_4285-7insTTT XP_016864668.1:n.4285-8_4285-7insTTT
XM_017009180.1:c.5380-8_5380-7insTTT XP_016864669.1:n.5380-8_5380-7insTTT
XM_017009181.1:c.5380-8_5380-7insTTT XP_016864670.1:n.5380-8_5380-7insTTT
XM_017009182.1:c.5380-8_5380-7insTTT XP_016864671.1:n.5380-8_5380-7insTTT
XM_017009183.1:c.5380-8_5380-7insTTT XP_016864672.1:n.5380-8_5380-7insTTT
XM_017009184.1:c.5380-8_5380-7insTTT XP_016864673.1:n.5380-8_5380-7insTTT
XM_017009185.1:c.469-8_469-7insTTT XP_016864674.1:n.469-8_469-7insTTT
XM_017009186.1:c.22-8_22-7insTTT XP_016864675.1:n.22-8_22-7insTTT
XM_017009187.1:c.5380-8_5380-7insTTT XP_016864676.1:n.5380-8_5380-7insTTT
XM_024454388.1:c.4285-8_4285-7insTTT XP_024310156.1:n.4285-8_4285-7insTTT
XM_024454389.1:c.3874-8_3874-7insTTT XP_024310157.1:n.3874-8_3874-7insTTT
XR_001742034.1:n.5397-8_5397-7insTTT
XR_001742035.1:n.5397-8_5397-7insTTT
NM_001369.3:c.5272-8_5272-7insTTT MANE Select NP_001360.1:n.5272-8_5272-7insTTT