Canonical Allele Identifier: CA1073395365

Gene: DNAH5

Linked Data

• gnomAD v3: 5-13841940-T-TAA
• gnomAD v4: 5-13841940-T-TAA

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13841941_13841942insAA , CM000667.2:g.13841941_13841942insAA	GRCh38
NC_000005.9:g.13842050_13842051insAA , CM000667.1:g.13842050_13842051insAA	GRCh37
NC_000005.8:g.13895050_13895051insAA	NCBI36
NG_013081.1:g.107540_107541insTT
NG_013081.2:g.107540_107541insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.5272-37_5272-36insTT MANE Select	ENSP00000265104.4:n.5272-37_5272-36insTT
ENST00000681290.1:c.5227-37_5227-36insTT	ENSP00000505288.1:n.5227-37_5227-36insTT
ENST00000265104.4:c.5272-37_5272-36insTT	ENSP00000265104.4:n.5272-37_5272-36insTT
NM_001369.2:c.5272-37_5272-36insTT	NP_001360.1:n.5272-37_5272-36insTT
XM_005248262.2:c.5227-37_5227-36insTT	XP_005248319.1:n.5227-37_5227-36insTT
XM_011513990.1:c.5272-37_5272-36insTT	XP_011512292.1:n.5272-37_5272-36insTT
XR_925598.1:n.5479-37_5479-36insTT
XM_005248262.3:c.5380-37_5380-36insTT	XP_005248319.2:n.5380-37_5380-36insTT
XM_017009177.1:c.5380-37_5380-36insTT	XP_016864666.1:n.5380-37_5380-36insTT
XM_017009178.1:c.4285-37_4285-36insTT	XP_016864667.1:n.4285-37_4285-36insTT
XM_017009179.2:c.4285-37_4285-36insTT	XP_016864668.1:n.4285-37_4285-36insTT
XM_017009180.1:c.5380-37_5380-36insTT	XP_016864669.1:n.5380-37_5380-36insTT
XM_017009181.1:c.5380-37_5380-36insTT	XP_016864670.1:n.5380-37_5380-36insTT
XM_017009182.1:c.5380-37_5380-36insTT	XP_016864671.1:n.5380-37_5380-36insTT
XM_017009183.1:c.5380-37_5380-36insTT	XP_016864672.1:n.5380-37_5380-36insTT
XM_017009184.1:c.5380-37_5380-36insTT	XP_016864673.1:n.5380-37_5380-36insTT
XM_017009185.1:c.469-37_469-36insTT	XP_016864674.1:n.469-37_469-36insTT
XM_017009186.1:c.22-37_22-36insTT	XP_016864675.1:n.22-37_22-36insTT
XM_017009187.1:c.5380-37_5380-36insTT	XP_016864676.1:n.5380-37_5380-36insTT
XM_024454388.1:c.4285-37_4285-36insTT	XP_024310156.1:n.4285-37_4285-36insTT
XM_024454389.1:c.3874-37_3874-36insTT	XP_024310157.1:n.3874-37_3874-36insTT
XR_001742034.1:n.5397-37_5397-36insTT
XR_001742035.1:n.5397-37_5397-36insTT
NM_001369.3:c.5272-37_5272-36insTT MANE Select	NP_001360.1:n.5272-37_5272-36insTT