Canonical Allele Identifier: CA1693539042

Gene: DNAH11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21558780A= , CM000669.2:g.21558780A=	GRCh38
NC_000007.13:g.21598398A= , CM000669.1:g.21598398A=	GRCh37
NC_000007.12:g.21564923A=	NCBI36
NG_012886.2:g.20566A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.496-22A= MANE Select	ENSP00000475939.1:n.496-22A=
ENST00000328843.10:c.496-22A=	ENSP00000330671.7:n.496-22A=
ENST00000409508.7:c.496-22A=	ENSP00000475939.1:n.496-22A=
ENST00000620169.4:c.496-22A=	ENSP00000481693.1:n.496-22A=
NM_001277115.1:c.496-22A=	NP_001264044.1:n.496-22A=
NM_001277115.2:c.496-22A= MANE Select	NP_001264044.1:n.496-22A=