Canonical Allele Identifier: CA2673274529

Gene: DNAH5

Linked Data

• gnomAD v4: 5-13841930-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13841930_13841931insG , CM000667.2:g.13841930_13841931insG	GRCh38
NC_000005.9:g.13842039_13842040insG , CM000667.1:g.13842039_13842040insG	GRCh37
NC_000005.8:g.13895039_13895040insG	NCBI36
NG_013081.1:g.107550_107551insC
NG_013081.2:g.107550_107551insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.5272-27_5272-26insC MANE Select	ENSP00000265104.4:n.5272-27_5272-26insC
ENST00000681290.1:c.5227-27_5227-26insC	ENSP00000505288.1:n.5227-27_5227-26insC
ENST00000265104.4:c.5272-27_5272-26insC	ENSP00000265104.4:n.5272-27_5272-26insC
NM_001369.2:c.5272-27_5272-26insC	NP_001360.1:n.5272-27_5272-26insC
XM_005248262.2:c.5227-27_5227-26insC	XP_005248319.1:n.5227-27_5227-26insC
XM_011513990.1:c.5272-27_5272-26insC	XP_011512292.1:n.5272-27_5272-26insC
XR_925598.1:n.5479-27_5479-26insC
XM_005248262.3:c.5380-27_5380-26insC	XP_005248319.2:n.5380-27_5380-26insC
XM_017009177.1:c.5380-27_5380-26insC	XP_016864666.1:n.5380-27_5380-26insC
XM_017009178.1:c.4285-27_4285-26insC	XP_016864667.1:n.4285-27_4285-26insC
XM_017009179.2:c.4285-27_4285-26insC	XP_016864668.1:n.4285-27_4285-26insC
XM_017009180.1:c.5380-27_5380-26insC	XP_016864669.1:n.5380-27_5380-26insC
XM_017009181.1:c.5380-27_5380-26insC	XP_016864670.1:n.5380-27_5380-26insC
XM_017009182.1:c.5380-27_5380-26insC	XP_016864671.1:n.5380-27_5380-26insC
XM_017009183.1:c.5380-27_5380-26insC	XP_016864672.1:n.5380-27_5380-26insC
XM_017009184.1:c.5380-27_5380-26insC	XP_016864673.1:n.5380-27_5380-26insC
XM_017009185.1:c.469-27_469-26insC	XP_016864674.1:n.469-27_469-26insC
XM_017009186.1:c.22-27_22-26insC	XP_016864675.1:n.22-27_22-26insC
XM_017009187.1:c.5380-27_5380-26insC	XP_016864676.1:n.5380-27_5380-26insC
XM_024454388.1:c.4285-27_4285-26insC	XP_024310156.1:n.4285-27_4285-26insC
XM_024454389.1:c.3874-27_3874-26insC	XP_024310157.1:n.3874-27_3874-26insC
XR_001742034.1:n.5397-27_5397-26insC
XR_001742035.1:n.5397-27_5397-26insC
NM_001369.3:c.5272-27_5272-26insC MANE Select	NP_001360.1:n.5272-27_5272-26insC