Canonical Allele Identifier: CA1693571452

Gene: DNAH11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21619088_21619089delinsTC , CM000669.2:g.21619088_21619089delinsTC	GRCh38
NC_000007.13:g.21658706_21658707delinsTC , CM000669.1:g.21658706_21658707delinsTC	GRCh37
NC_000007.12:g.21625231_21625232delinsTC	NCBI36
NG_012886.2:g.80874_80875delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.4255-12_4255-11delinsTC MANE Select	ENSP00000475939.1:n.4255-12_4255-11delinsTC
ENST00000328843.10:c.4270-12_4270-11delinsTC	ENSP00000330671.7:n.4270-12_4270-11delinsTC
ENST00000409508.7:c.4255-12_4255-11delinsTC	ENSP00000475939.1:n.4255-12_4255-11delinsTC
ENST00000465593.1:n.281-12_281-11delinsTC
ENST00000620169.4:c.4270-12_4270-11delinsTC	ENSP00000481693.1:n.4270-12_4270-11delinsTC
NM_001277115.1:c.4255-12_4255-11delinsTC	NP_001264044.1:n.4255-12_4255-11delinsTC
NM_001277115.2:c.4255-12_4255-11delinsTC MANE Select	NP_001264044.1:n.4255-12_4255-11delinsTC