Canonical Allele Identifier: CA2673274345
Gene: DNAH5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13841911_13841912insGA , CM000667.2:g.13841911_13841912insGA GRCh38
NC_000005.9:g.13842020_13842021insGA , CM000667.1:g.13842020_13842021insGA GRCh37
NC_000005.8:g.13895020_13895021insGA NCBI36
NG_013081.1:g.107569_107570insTC
NG_013081.2:g.107569_107570insTC

Transcript Alleles

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