Canonical Allele Identifier: CA1693571619

Gene: DNAH11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21619152G= , CM000669.2:g.21619152G=	GRCh38
NC_000007.13:g.21658770G= , CM000669.1:g.21658770G=	GRCh37
NC_000007.12:g.21625295G=	NCBI36
NG_012886.2:g.80938G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.4307G= MANE Select	ENSP00000475939.1:p.Arg1436=
ENST00000328843.10:c.4322G=	ENSP00000330671.7:p.Arg1441=
ENST00000409508.7:c.4307G=	ENSP00000475939.1:p.Arg1436=
ENST00000465593.1:n.333G=
ENST00000620169.4:c.4322G=	ENSP00000481693.1:p.Arg1441=
NM_001277115.1:c.4307G=	NP_001264044.1:p.Arg1436=
NM_001277115.2:c.4307G= MANE Select	NP_001264044.1:p.Arg1436=