Canonical Allele Identifier: CA1528463592

Gene: DNAH5

Linked Data

• dbSNP Id: rs1765252366

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13842007_13842008insCCCCAAACTTGAA , CM000667.2:g.13842007_13842008insCCCCAAACTTGAA	GRCh38
NC_000005.9:g.13842116_13842117insCCCCAAACTTGAA , CM000667.1:g.13842116_13842117insCCCCAAACTTGAA	GRCh37
NC_000005.8:g.13895116_13895117insCCCCAAACTTGAA	NCBI36
NG_013081.1:g.107473_107474insTTCAAGTTTGGGG
NG_013081.2:g.107473_107474insTTCAAGTTTGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.5272-104_5272-103insTTCAAGTTTGGGG MANE Select	ENSP00000265104.4:n.5272-104_5272-103insTTCAAGTTTGGGG
ENST00000681290.1:c.5227-104_5227-103insTTCAAGTTTGGGG	ENSP00000505288.1:n.5227-104_5227-103insTTCAAGTTTGGGG
ENST00000265104.4:c.5272-104_5272-103insTTCAAGTTTGGGG	ENSP00000265104.4:n.5272-104_5272-103insTTCAAGTTTGGGG
NM_001369.2:c.5272-104_5272-103insTTCAAGTTTGGGG	NP_001360.1:n.5272-104_5272-103insTTCAAGTTTGGGG
XM_005248262.2:c.5227-104_5227-103insTTCAAGTTTGGGG	XP_005248319.1:n.5227-104_5227-103insTTCAAGTTTGGGG
XM_011513990.1:c.5272-104_5272-103insTTCAAGTTTGGGG	XP_011512292.1:n.5272-104_5272-103insTTCAAGTTTGGGG
XR_925598.1:n.5479-104_5479-103insTTCAAGTTTGGGG
XM_005248262.3:c.5380-104_5380-103insTTCAAGTTTGGGG	XP_005248319.2:n.5380-104_5380-103insTTCAAGTTTGGGG
XM_017009177.1:c.5380-104_5380-103insTTCAAGTTTGGGG	XP_016864666.1:n.5380-104_5380-103insTTCAAGTTTGGGG
XM_017009178.1:c.4285-104_4285-103insTTCAAGTTTGGGG	XP_016864667.1:n.4285-104_4285-103insTTCAAGTTTGGGG
XM_017009179.2:c.4285-104_4285-103insTTCAAGTTTGGGG	XP_016864668.1:n.4285-104_4285-103insTTCAAGTTTGGGG
XM_017009180.1:c.5380-104_5380-103insTTCAAGTTTGGGG	XP_016864669.1:n.5380-104_5380-103insTTCAAGTTTGGGG
XM_017009181.1:c.5380-104_5380-103insTTCAAGTTTGGGG	XP_016864670.1:n.5380-104_5380-103insTTCAAGTTTGGGG
XM_017009182.1:c.5380-104_5380-103insTTCAAGTTTGGGG	XP_016864671.1:n.5380-104_5380-103insTTCAAGTTTGGGG
XM_017009183.1:c.5380-104_5380-103insTTCAAGTTTGGGG	XP_016864672.1:n.5380-104_5380-103insTTCAAGTTTGGGG
XM_017009184.1:c.5380-104_5380-103insTTCAAGTTTGGGG	XP_016864673.1:n.5380-104_5380-103insTTCAAGTTTGGGG
XM_017009185.1:c.469-104_469-103insTTCAAGTTTGGGG	XP_016864674.1:n.469-104_469-103insTTCAAGTTTGGGG
XM_017009186.1:c.22-104_22-103insTTCAAGTTTGGGG	XP_016864675.1:n.22-104_22-103insTTCAAGTTTGGGG
XM_017009187.1:c.5380-104_5380-103insTTCAAGTTTGGGG	XP_016864676.1:n.5380-104_5380-103insTTCAAGTTTGGGG
XM_024454388.1:c.4285-104_4285-103insTTCAAGTTTGGGG	XP_024310156.1:n.4285-104_4285-103insTTCAAGTTTGGGG
XM_024454389.1:c.3874-104_3874-103insTTCAAGTTTGGGG	XP_024310157.1:n.3874-104_3874-103insTTCAAGTTTGGGG
XR_001742034.1:n.5397-104_5397-103insTTCAAGTTTGGGG
XR_001742035.1:n.5397-104_5397-103insTTCAAGTTTGGGG
NM_001369.3:c.5272-104_5272-103insTTCAAGTTTGGGG MANE Select	NP_001360.1:n.5272-104_5272-103insTTCAAGTTTGGGG