Canonical Allele Identifier: CA1693712639

Gene: DNAH11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21880747_21880748delinsCT , CM000669.2:g.21880747_21880748delinsCT	GRCh38
NC_000007.13:g.21920365_21920366delinsCT , CM000669.1:g.21920365_21920366delinsCT	GRCh37
NC_000007.12:g.21886890_21886891delinsCT	NCBI36
NG_012886.2:g.342533_342534delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.12241_12242delinsCT MANE Select	ENSP00000475939.1:p.Leu4081=
ENST00000328843.10:c.12262_12263delinsCT	ENSP00000330671.7:p.Leu4088=
ENST00000409508.7:c.12241_12242delinsCT	ENSP00000475939.1:p.Leu4081=
ENST00000620169.4:c.12262_12263delinsCT	ENSP00000481693.1:p.Leu4088=
NM_001277115.1:c.12241_12242delinsCT	NP_001264044.1:p.Leu4081=
NM_001277115.2:c.12241_12242delinsCT MANE Select	NP_001264044.1:p.Leu4081=