Canonical Allele Identifier: CA1693709013

Gene: DNAH11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21854386A= , CM000669.2:g.21854386A=	GRCh38
NC_000007.13:g.21894004A= , CM000669.1:g.21894004A=	GRCh37
NC_000007.12:g.21860529A=	NCBI36
NG_012886.2:g.316172A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000409508.8:c.11133A= MANE Select	ENSP00000475939.1:p.Arg3711=
ENST00000328843.10:c.11154A=	ENSP00000330671.7:p.Arg3718=
ENST00000409508.7:c.11133A=	ENSP00000475939.1:p.Arg3711=
ENST00000421290.1:n.316A=
ENST00000607413.5:n.396A=
ENST00000620169.4:c.11154A=	ENSP00000481693.1:p.Arg3718=
NM_001277115.1:c.11133A=	NP_001264044.1:p.Arg3711=
NM_001277115.2:c.11133A= MANE Select	NP_001264044.1:p.Arg3711=