Canonical Allele Identifier: CA1693713220

Gene: DNAH11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21881263_21881264delinsCT , CM000669.2:g.21881263_21881264delinsCT	GRCh38
NC_000007.13:g.21920881_21920882delinsCT , CM000669.1:g.21920881_21920882delinsCT	GRCh37
NC_000007.12:g.21887406_21887407delinsCT	NCBI36
NG_012886.2:g.343049_343050delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.12387+370_12387+371delinsCT MANE Select	ENSP00000475939.1:n.12387+370_12387+371delinsCT
ENST00000328843.10:c.12408+370_12408+371delinsCT	ENSP00000330671.7:n.12408+370_12408+371delinsCT
ENST00000409508.7:c.12387+370_12387+371delinsCT	ENSP00000475939.1:n.12387+370_12387+371delinsCT
ENST00000620169.4:c.12408+370_12408+371delinsCT	ENSP00000481693.1:n.12408+370_12408+371delinsCT
NM_001277115.1:c.12387+370_12387+371delinsCT	NP_001264044.1:n.12387+370_12387+371delinsCT
NM_001277115.2:c.12387+370_12387+371delinsCT MANE Select	NP_001264044.1:n.12387+370_12387+371delinsCT