Canonical Allele Identifier: CA2673274552

Gene: DNAH5

Linked Data

• gnomAD v4: 5-13841936-A-AAAAAAAAAAG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13841937_13841938insAAAAAAAAGA , CM000667.2:g.13841937_13841938insAAAAAAAAGA	GRCh38
NC_000005.9:g.13842046_13842047insAAAAAAAAGA , CM000667.1:g.13842046_13842047insAAAAAAAAGA	GRCh37
NC_000005.8:g.13895046_13895047insAAAAAAAAGA	NCBI36
NG_013081.1:g.107544_107545insCTTTTTTTTT
NG_013081.2:g.107544_107545insCTTTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.5272-33_5272-32insCTTTTTTTTT MANE Select	ENSP00000265104.4:n.5272-33_5272-32insCTTTTTTTTT
ENST00000681290.1:c.5227-33_5227-32insCTTTTTTTTT	ENSP00000505288.1:n.5227-33_5227-32insCTTTTTTTTT
ENST00000265104.4:c.5272-33_5272-32insCTTTTTTTTT	ENSP00000265104.4:n.5272-33_5272-32insCTTTTTTTTT
NM_001369.2:c.5272-33_5272-32insCTTTTTTTTT	NP_001360.1:n.5272-33_5272-32insCTTTTTTTTT
XM_005248262.2:c.5227-33_5227-32insCTTTTTTTTT	XP_005248319.1:n.5227-33_5227-32insCTTTTTTTTT
XM_011513990.1:c.5272-33_5272-32insCTTTTTTTTT	XP_011512292.1:n.5272-33_5272-32insCTTTTTTTTT
XR_925598.1:n.5479-33_5479-32insCTTTTTTTTT
XM_005248262.3:c.5380-33_5380-32insCTTTTTTTTT	XP_005248319.2:n.5380-33_5380-32insCTTTTTTTTT
XM_017009177.1:c.5380-33_5380-32insCTTTTTTTTT	XP_016864666.1:n.5380-33_5380-32insCTTTTTTTTT
XM_017009178.1:c.4285-33_4285-32insCTTTTTTTTT	XP_016864667.1:n.4285-33_4285-32insCTTTTTTTTT
XM_017009179.2:c.4285-33_4285-32insCTTTTTTTTT	XP_016864668.1:n.4285-33_4285-32insCTTTTTTTTT
XM_017009180.1:c.5380-33_5380-32insCTTTTTTTTT	XP_016864669.1:n.5380-33_5380-32insCTTTTTTTTT
XM_017009181.1:c.5380-33_5380-32insCTTTTTTTTT	XP_016864670.1:n.5380-33_5380-32insCTTTTTTTTT
XM_017009182.1:c.5380-33_5380-32insCTTTTTTTTT	XP_016864671.1:n.5380-33_5380-32insCTTTTTTTTT
XM_017009183.1:c.5380-33_5380-32insCTTTTTTTTT	XP_016864672.1:n.5380-33_5380-32insCTTTTTTTTT
XM_017009184.1:c.5380-33_5380-32insCTTTTTTTTT	XP_016864673.1:n.5380-33_5380-32insCTTTTTTTTT
XM_017009185.1:c.469-33_469-32insCTTTTTTTTT	XP_016864674.1:n.469-33_469-32insCTTTTTTTTT
XM_017009186.1:c.22-33_22-32insCTTTTTTTTT	XP_016864675.1:n.22-33_22-32insCTTTTTTTTT
XM_017009187.1:c.5380-33_5380-32insCTTTTTTTTT	XP_016864676.1:n.5380-33_5380-32insCTTTTTTTTT
XM_024454388.1:c.4285-33_4285-32insCTTTTTTTTT	XP_024310156.1:n.4285-33_4285-32insCTTTTTTTTT
XM_024454389.1:c.3874-33_3874-32insCTTTTTTTTT	XP_024310157.1:n.3874-33_3874-32insCTTTTTTTTT
XR_001742034.1:n.5397-33_5397-32insCTTTTTTTTT
XR_001742035.1:n.5397-33_5397-32insCTTTTTTTTT
NM_001369.3:c.5272-33_5272-32insCTTTTTTTTT MANE Select	NP_001360.1:n.5272-33_5272-32insCTTTTTTTTT