Canonical Allele Identifier: CA1693712662

Gene: DNAH11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21880760G= , CM000669.2:g.21880760G=	GRCh38
NC_000007.13:g.21920378G= , CM000669.1:g.21920378G=	GRCh37
NC_000007.12:g.21886903G=	NCBI36
NG_012886.2:g.342546G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000409508.8:c.12254G= MANE Select	ENSP00000475939.1:p.Cys4085=
ENST00000328843.10:c.12275G=	ENSP00000330671.7:p.Cys4092=
ENST00000409508.7:c.12254G=	ENSP00000475939.1:p.Cys4085=
ENST00000620169.4:c.12275G=	ENSP00000481693.1:p.Cys4092=
NM_001277115.1:c.12254G=	NP_001264044.1:p.Cys4085=
NM_001277115.2:c.12254G= MANE Select	NP_001264044.1:p.Cys4085=