Canonical Allele Identifier: CA1693539309

Gene: DNAH11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21558884A= , CM000669.2:g.21558884A=	GRCh38
NC_000007.13:g.21598502A= , CM000669.1:g.21598502A=	GRCh37
NC_000007.12:g.21565027A=	NCBI36
NG_012886.2:g.20670A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000409508.8:c.578A= MANE Select	ENSP00000475939.1:p.Glu193=
ENST00000328843.10:c.578A=	ENSP00000330671.7:p.Glu193=
ENST00000409508.7:c.578A=	ENSP00000475939.1:p.Glu193=
ENST00000620169.4:c.578A=	ENSP00000481693.1:p.Glu193=
NM_001277115.1:c.578A=	NP_001264044.1:p.Glu193=
NM_001277115.2:c.578A= MANE Select	NP_001264044.1:p.Glu193=