Canonical Allele Identifier: CA1693712664

Gene: DNAH11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21880761C= , CM000669.2:g.21880761C=	GRCh38
NC_000007.13:g.21920379C= , CM000669.1:g.21920379C=	GRCh37
NC_000007.12:g.21886904C=	NCBI36
NG_012886.2:g.342547C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000409508.8:c.12255C= MANE Select	ENSP00000475939.1:p.Cys4085=
ENST00000328843.10:c.12276C=	ENSP00000330671.7:p.Cys4092=
ENST00000409508.7:c.12255C=	ENSP00000475939.1:p.Cys4085=
ENST00000620169.4:c.12276C=	ENSP00000481693.1:p.Cys4092=
NM_001277115.1:c.12255C=	NP_001264044.1:p.Cys4085=
NM_001277115.2:c.12255C= MANE Select	NP_001264044.1:p.Cys4085=