Canonical Allele Identifier: CA2673274534

Gene: DNAH5

Linked Data

• gnomAD v4: 5-13841934-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13841934_13841935insG , CM000667.2:g.13841934_13841935insG	GRCh38
NC_000005.9:g.13842043_13842044insG , CM000667.1:g.13842043_13842044insG	GRCh37
NC_000005.8:g.13895043_13895044insG	NCBI36
NG_013081.1:g.107546_107547insC
NG_013081.2:g.107546_107547insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.5272-31_5272-30insC MANE Select	ENSP00000265104.4:n.5272-31_5272-30insC
ENST00000681290.1:c.5227-31_5227-30insC	ENSP00000505288.1:n.5227-31_5227-30insC
ENST00000265104.4:c.5272-31_5272-30insC	ENSP00000265104.4:n.5272-31_5272-30insC
NM_001369.2:c.5272-31_5272-30insC	NP_001360.1:n.5272-31_5272-30insC
XM_005248262.2:c.5227-31_5227-30insC	XP_005248319.1:n.5227-31_5227-30insC
XM_011513990.1:c.5272-31_5272-30insC	XP_011512292.1:n.5272-31_5272-30insC
XR_925598.1:n.5479-31_5479-30insC
XM_005248262.3:c.5380-31_5380-30insC	XP_005248319.2:n.5380-31_5380-30insC
XM_017009177.1:c.5380-31_5380-30insC	XP_016864666.1:n.5380-31_5380-30insC
XM_017009178.1:c.4285-31_4285-30insC	XP_016864667.1:n.4285-31_4285-30insC
XM_017009179.2:c.4285-31_4285-30insC	XP_016864668.1:n.4285-31_4285-30insC
XM_017009180.1:c.5380-31_5380-30insC	XP_016864669.1:n.5380-31_5380-30insC
XM_017009181.1:c.5380-31_5380-30insC	XP_016864670.1:n.5380-31_5380-30insC
XM_017009182.1:c.5380-31_5380-30insC	XP_016864671.1:n.5380-31_5380-30insC
XM_017009183.1:c.5380-31_5380-30insC	XP_016864672.1:n.5380-31_5380-30insC
XM_017009184.1:c.5380-31_5380-30insC	XP_016864673.1:n.5380-31_5380-30insC
XM_017009185.1:c.469-31_469-30insC	XP_016864674.1:n.469-31_469-30insC
XM_017009186.1:c.22-31_22-30insC	XP_016864675.1:n.22-31_22-30insC
XM_017009187.1:c.5380-31_5380-30insC	XP_016864676.1:n.5380-31_5380-30insC
XM_024454388.1:c.4285-31_4285-30insC	XP_024310156.1:n.4285-31_4285-30insC
XM_024454389.1:c.3874-31_3874-30insC	XP_024310157.1:n.3874-31_3874-30insC
XR_001742034.1:n.5397-31_5397-30insC
XR_001742035.1:n.5397-31_5397-30insC
NM_001369.3:c.5272-31_5272-30insC MANE Select	NP_001360.1:n.5272-31_5272-30insC