Canonical Allele Identifier: CA1528463594

Gene: DNAH5

Linked Data

• dbSNP Id: rs1765252726

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13842009_13842010insGGAAG , CM000667.2:g.13842009_13842010insGGAAG	GRCh38
NC_000005.9:g.13842118_13842119insGGAAG , CM000667.1:g.13842118_13842119insGGAAG	GRCh37
NC_000005.8:g.13895118_13895119insGGAAG	NCBI36
NG_013081.1:g.107471_107472insCTTCC
NG_013081.2:g.107471_107472insCTTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.5272-106_5272-105insCTTCC MANE Select	ENSP00000265104.4:n.5272-106_5272-105insCTTCC
ENST00000681290.1:c.5227-106_5227-105insCTTCC	ENSP00000505288.1:n.5227-106_5227-105insCTTCC
ENST00000265104.4:c.5272-106_5272-105insCTTCC	ENSP00000265104.4:n.5272-106_5272-105insCTTCC
NM_001369.2:c.5272-106_5272-105insCTTCC	NP_001360.1:n.5272-106_5272-105insCTTCC
XM_005248262.2:c.5227-106_5227-105insCTTCC	XP_005248319.1:n.5227-106_5227-105insCTTCC
XM_011513990.1:c.5272-106_5272-105insCTTCC	XP_011512292.1:n.5272-106_5272-105insCTTCC
XR_925598.1:n.5479-106_5479-105insCTTCC
XM_005248262.3:c.5380-106_5380-105insCTTCC	XP_005248319.2:n.5380-106_5380-105insCTTCC
XM_017009177.1:c.5380-106_5380-105insCTTCC	XP_016864666.1:n.5380-106_5380-105insCTTCC
XM_017009178.1:c.4285-106_4285-105insCTTCC	XP_016864667.1:n.4285-106_4285-105insCTTCC
XM_017009179.2:c.4285-106_4285-105insCTTCC	XP_016864668.1:n.4285-106_4285-105insCTTCC
XM_017009180.1:c.5380-106_5380-105insCTTCC	XP_016864669.1:n.5380-106_5380-105insCTTCC
XM_017009181.1:c.5380-106_5380-105insCTTCC	XP_016864670.1:n.5380-106_5380-105insCTTCC
XM_017009182.1:c.5380-106_5380-105insCTTCC	XP_016864671.1:n.5380-106_5380-105insCTTCC
XM_017009183.1:c.5380-106_5380-105insCTTCC	XP_016864672.1:n.5380-106_5380-105insCTTCC
XM_017009184.1:c.5380-106_5380-105insCTTCC	XP_016864673.1:n.5380-106_5380-105insCTTCC
XM_017009185.1:c.469-106_469-105insCTTCC	XP_016864674.1:n.469-106_469-105insCTTCC
XM_017009186.1:c.22-106_22-105insCTTCC	XP_016864675.1:n.22-106_22-105insCTTCC
XM_017009187.1:c.5380-106_5380-105insCTTCC	XP_016864676.1:n.5380-106_5380-105insCTTCC
XM_024454388.1:c.4285-106_4285-105insCTTCC	XP_024310156.1:n.4285-106_4285-105insCTTCC
XM_024454389.1:c.3874-106_3874-105insCTTCC	XP_024310157.1:n.3874-106_3874-105insCTTCC
XR_001742034.1:n.5397-106_5397-105insCTTCC
XR_001742035.1:n.5397-106_5397-105insCTTCC
NM_001369.3:c.5272-106_5272-105insCTTCC MANE Select	NP_001360.1:n.5272-106_5272-105insCTTCC