Canonical Allele Identifier: CA2673274722

Gene: DNAH5

Linked Data

• gnomAD v4: 5-13844998-A-AAAC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13844999_13845000insACA , CM000667.2:g.13844999_13845000insACA	GRCh38
NC_000005.9:g.13845108_13845109insACA , CM000667.1:g.13845108_13845109insACA	GRCh37
NC_000005.8:g.13898108_13898109insACA	NCBI36
NG_013081.1:g.104482_104483insGTT
NG_013081.2:g.104482_104483insGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.5115-6_5115-5insGTT MANE Select	ENSP00000265104.4:n.5115-6_5115-5insGTT
ENST00000681290.1:c.5070-6_5070-5insGTT	ENSP00000505288.1:n.5070-6_5070-5insGTT
ENST00000265104.4:c.5115-6_5115-5insGTT	ENSP00000265104.4:n.5115-6_5115-5insGTT
NM_001369.2:c.5115-6_5115-5insGTT	NP_001360.1:n.5115-6_5115-5insGTT
XM_005248262.2:c.5070-6_5070-5insGTT	XP_005248319.1:n.5070-6_5070-5insGTT
XM_011513990.1:c.5115-6_5115-5insGTT	XP_011512292.1:n.5115-6_5115-5insGTT
XR_925598.1:n.5322-6_5322-5insGTT
XM_005248262.3:c.5223-6_5223-5insGTT	XP_005248319.2:n.5223-6_5223-5insGTT
XM_017009177.1:c.5223-6_5223-5insGTT	XP_016864666.1:n.5223-6_5223-5insGTT
XM_017009178.1:c.4128-6_4128-5insGTT	XP_016864667.1:n.4128-6_4128-5insGTT
XM_017009179.2:c.4128-6_4128-5insGTT	XP_016864668.1:n.4128-6_4128-5insGTT
XM_017009180.1:c.5223-6_5223-5insGTT	XP_016864669.1:n.5223-6_5223-5insGTT
XM_017009181.1:c.5223-6_5223-5insGTT	XP_016864670.1:n.5223-6_5223-5insGTT
XM_017009182.1:c.5223-6_5223-5insGTT	XP_016864671.1:n.5223-6_5223-5insGTT
XM_017009183.1:c.5223-6_5223-5insGTT	XP_016864672.1:n.5223-6_5223-5insGTT
XM_017009184.1:c.5223-6_5223-5insGTT	XP_016864673.1:n.5223-6_5223-5insGTT
XM_017009185.1:c.312-6_312-5insGTT	XP_016864674.1:n.312-6_312-5insGTT
XM_017009186.1:c.22-3095_22-3094insGTT	XP_016864675.1:n.22-3095_22-3094insGTT
XM_017009187.1:c.5223-6_5223-5insGTT	XP_016864676.1:n.5223-6_5223-5insGTT
XM_024454388.1:c.4128-6_4128-5insGTT	XP_024310156.1:n.4128-6_4128-5insGTT
XM_024454389.1:c.3717-6_3717-5insGTT	XP_024310157.1:n.3717-6_3717-5insGTT
XR_001742034.1:n.5240-6_5240-5insGTT
XR_001742035.1:n.5240-6_5240-5insGTT
NM_001369.3:c.5115-6_5115-5insGTT MANE Select	NP_001360.1:n.5115-6_5115-5insGTT