Canonical Allele Identifier: CA2765346679

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13691846_13691847insC , CM000667.2:g.13691846_13691847insC	GRCh38
NC_000005.9:g.13691955_13691956insC , CM000667.1:g.13691955_13691956insC	GRCh37
NC_000005.8:g.13744955_13744956insC	NCBI36
NG_013081.1:g.257634_257635insG
NG_013081.2:g.257634_257635insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683611.1:n.1345_1346insG
ENST00000265104.5:c.*137_*138insG MANE Select	ENSP00000265104.4:n.*137_*138insG
ENST00000681290.1:c.*137_*138insG	ENSP00000505288.1:n.*137_*138insG
ENST00000265104.4:c.*137_*138insG	ENSP00000265104.4:n.*137_*138insG
NM_001369.2:c.*137_*138insG	NP_001360.1:n.*137_*138insG
XM_005248262.2:c.*137_*138insG	XP_005248319.1:n.*137_*138insG
XM_005248262.3:c.*137_*138insG	XP_005248319.2:n.*137_*138insG
XM_017009177.1:c.*137_*138insG	XP_016864666.1:n.*137_*138insG
XM_017009178.1:c.*137_*138insG	XP_016864667.1:n.*137_*138insG
XM_017009179.2:c.*137_*138insG	XP_016864668.1:n.*137_*138insG
XM_017009185.1:c.*137_*138insG	XP_016864674.1:n.*137_*138insG
XM_017009186.1:c.*137_*138insG	XP_016864675.1:n.*137_*138insG
XM_017009188.1:c.*137_*138insG	XP_016864677.1:n.*137_*138insG
XM_024454388.1:c.*137_*138insG	XP_024310156.1:n.*137_*138insG
XM_024454389.1:c.*137_*138insG	XP_024310157.1:n.*137_*138insG
NM_001369.3:c.*137_*138insG MANE Select	NP_001360.1:n.*137_*138insG