Canonical Allele Identifier: CA1073394790

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13841936_13841937insGAAAAAAACAAAAAAAAAAAAAAAAAA , CM000667.2:g.13841936_13841937insGAAAAAAACAAAAAAAAAAAAAAAAAA	GRCh38
NC_000005.9:g.13842045_13842046insGAAAAAAACAAAAAAAAAAAAAAAAAA , CM000667.1:g.13842045_13842046insGAAAAAAACAAAAAAAAAAAAAAAAAA	GRCh37
NC_000005.8:g.13895045_13895046insGAAAAAAACAAAAAAAAAAAAAAAAAA	NCBI36
NG_013081.1:g.107563_107564insTTTTTTTCTTTTTTTTTTTTTTTTTTG
NG_013081.2:g.107563_107564insTTTTTTTCTTTTTTTTTTTTTTTTTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.5272-14_5272-13insTTTTTTTCTTTTTTTTTTTTTTTTTTG MANE Select	ENSP00000265104.4:n.5272-14_5272-13insTTTTTTTCTTTTTTTTTTTTTTT...
ENST00000681290.1:c.5227-14_5227-13insTTTTTTTCTTTTTTTTTTTTTTTTTTG	ENSP00000505288.1:n.5227-14_5227-13insTTTTTTTCTTTTTTTTTTTTTTT...
ENST00000265104.4:c.5272-14_5272-13insTTTTTTTCTTTTTTTTTTTTTTTTTTG	ENSP00000265104.4:n.5272-14_5272-13insTTTTTTTCTTTTTTTTTTTTTTT...
NM_001369.2:c.5272-14_5272-13insTTTTTTTCTTTTTTTTTTTTTTTTTTG	NP_001360.1:n.5272-14_5272-13insTTTTTTTCTTTTTTTTTTTTTTTTTTG
XM_005248262.2:c.5227-14_5227-13insTTTTTTTCTTTTTTTTTTTTTTTTTTG	XP_005248319.1:n.5227-14_5227-13insTTTTTTTCTTTTTTTTTTTTTTTTTT...
XM_011513990.1:c.5272-14_5272-13insTTTTTTTCTTTTTTTTTTTTTTTTTTG	XP_011512292.1:n.5272-14_5272-13insTTTTTTTCTTTTTTTTTTTTTTTTTT...
XR_925598.1:n.5479-14_5479-13insTTTTTTTCTTTTTTTTTTTTTTTTTTG
XM_005248262.3:c.5380-14_5380-13insTTTTTTTCTTTTTTTTTTTTTTTTTTG	XP_005248319.2:n.5380-14_5380-13insTTTTTTTCTTTTTTTTTTTTTTTTTT...
XM_017009177.1:c.5380-14_5380-13insTTTTTTTCTTTTTTTTTTTTTTTTTTG	XP_016864666.1:n.5380-14_5380-13insTTTTTTTCTTTTTTTTTTTTTTTTTT...
XM_017009178.1:c.4285-14_4285-13insTTTTTTTCTTTTTTTTTTTTTTTTTTG	XP_016864667.1:n.4285-14_4285-13insTTTTTTTCTTTTTTTTTTTTTTTTTT...
XM_017009179.2:c.4285-14_4285-13insTTTTTTTCTTTTTTTTTTTTTTTTTTG	XP_016864668.1:n.4285-14_4285-13insTTTTTTTCTTTTTTTTTTTTTTTTTT...
XM_017009180.1:c.5380-14_5380-13insTTTTTTTCTTTTTTTTTTTTTTTTTTG	XP_016864669.1:n.5380-14_5380-13insTTTTTTTCTTTTTTTTTTTTTTTTTT...
XM_017009181.1:c.5380-14_5380-13insTTTTTTTCTTTTTTTTTTTTTTTTTTG	XP_016864670.1:n.5380-14_5380-13insTTTTTTTCTTTTTTTTTTTTTTTTTT...
XM_017009182.1:c.5380-14_5380-13insTTTTTTTCTTTTTTTTTTTTTTTTTTG	XP_016864671.1:n.5380-14_5380-13insTTTTTTTCTTTTTTTTTTTTTTTTTT...
XM_017009183.1:c.5380-14_5380-13insTTTTTTTCTTTTTTTTTTTTTTTTTTG	XP_016864672.1:n.5380-14_5380-13insTTTTTTTCTTTTTTTTTTTTTTTTTT...
XM_017009184.1:c.5380-14_5380-13insTTTTTTTCTTTTTTTTTTTTTTTTTTG	XP_016864673.1:n.5380-14_5380-13insTTTTTTTCTTTTTTTTTTTTTTTTTT...
XM_017009185.1:c.469-14_469-13insTTTTTTTCTTTTTTTTTTTTTTTTTTG	XP_016864674.1:n.469-14_469-13insTTTTTTTCTTTTTTTTTTTTTTTTTTG
XM_017009186.1:c.22-14_22-13insTTTTTTTCTTTTTTTTTTTTTTTTTTG	XP_016864675.1:n.22-14_22-13insTTTTTTTCTTTTTTTTTTTTTTTTTTG
XM_017009187.1:c.5380-14_5380-13insTTTTTTTCTTTTTTTTTTTTTTTTTTG	XP_016864676.1:n.5380-14_5380-13insTTTTTTTCTTTTTTTTTTTTTTTTTT...
XM_024454388.1:c.4285-14_4285-13insTTTTTTTCTTTTTTTTTTTTTTTTTTG	XP_024310156.1:n.4285-14_4285-13insTTTTTTTCTTTTTTTTTTTTTTTTTT...
XM_024454389.1:c.3874-14_3874-13insTTTTTTTCTTTTTTTTTTTTTTTTTTG	XP_024310157.1:n.3874-14_3874-13insTTTTTTTCTTTTTTTTTTTTTTTTTT...
XR_001742034.1:n.5397-14_5397-13insTTTTTTTCTTTTTTTTTTTTTTTTTTG
XR_001742035.1:n.5397-14_5397-13insTTTTTTTCTTTTTTTTTTTTTTTTTTG
NM_001369.3:c.5272-14_5272-13insTTTTTTTCTTTTTTTTTTTTTTTTTTG MANE Select	NP_001360.1:n.5272-14_5272-13insTTTTTTTCTTTTTTTTTTTTTTTTTTG