Canonical Allele Identifier: CA2673274565

Gene: DNAH5

Linked Data

• gnomAD v4: 5-13841943-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13841943_13841944insT , CM000667.2:g.13841943_13841944insT	GRCh38
NC_000005.9:g.13842052_13842053insT , CM000667.1:g.13842052_13842053insT	GRCh37
NC_000005.8:g.13895052_13895053insT	NCBI36
NG_013081.1:g.107537_107538insA
NG_013081.2:g.107537_107538insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.5272-40_5272-39insA MANE Select	ENSP00000265104.4:n.5272-40_5272-39insA
ENST00000681290.1:c.5227-40_5227-39insA	ENSP00000505288.1:n.5227-40_5227-39insA
ENST00000265104.4:c.5272-40_5272-39insA	ENSP00000265104.4:n.5272-40_5272-39insA
NM_001369.2:c.5272-40_5272-39insA	NP_001360.1:n.5272-40_5272-39insA
XM_005248262.2:c.5227-40_5227-39insA	XP_005248319.1:n.5227-40_5227-39insA
XM_011513990.1:c.5272-40_5272-39insA	XP_011512292.1:n.5272-40_5272-39insA
XR_925598.1:n.5479-40_5479-39insA
XM_005248262.3:c.5380-40_5380-39insA	XP_005248319.2:n.5380-40_5380-39insA
XM_017009177.1:c.5380-40_5380-39insA	XP_016864666.1:n.5380-40_5380-39insA
XM_017009178.1:c.4285-40_4285-39insA	XP_016864667.1:n.4285-40_4285-39insA
XM_017009179.2:c.4285-40_4285-39insA	XP_016864668.1:n.4285-40_4285-39insA
XM_017009180.1:c.5380-40_5380-39insA	XP_016864669.1:n.5380-40_5380-39insA
XM_017009181.1:c.5380-40_5380-39insA	XP_016864670.1:n.5380-40_5380-39insA
XM_017009182.1:c.5380-40_5380-39insA	XP_016864671.1:n.5380-40_5380-39insA
XM_017009183.1:c.5380-40_5380-39insA	XP_016864672.1:n.5380-40_5380-39insA
XM_017009184.1:c.5380-40_5380-39insA	XP_016864673.1:n.5380-40_5380-39insA
XM_017009185.1:c.469-40_469-39insA	XP_016864674.1:n.469-40_469-39insA
XM_017009186.1:c.22-40_22-39insA	XP_016864675.1:n.22-40_22-39insA
XM_017009187.1:c.5380-40_5380-39insA	XP_016864676.1:n.5380-40_5380-39insA
XM_024454388.1:c.4285-40_4285-39insA	XP_024310156.1:n.4285-40_4285-39insA
XM_024454389.1:c.3874-40_3874-39insA	XP_024310157.1:n.3874-40_3874-39insA
XR_001742034.1:n.5397-40_5397-39insA
XR_001742035.1:n.5397-40_5397-39insA
NM_001369.3:c.5272-40_5272-39insA MANE Select	NP_001360.1:n.5272-40_5272-39insA