Canonical Allele Identifier: CA1693538963

Gene: DNAH11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21558724C= , CM000669.2:g.21558724C=	GRCh38
NC_000007.13:g.21598342C= , CM000669.1:g.21598342C=	GRCh37
NC_000007.12:g.21564867C=	NCBI36
NG_012886.2:g.20510C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.496-78C= MANE Select	ENSP00000475939.1:n.496-78C=
ENST00000328843.10:c.496-78C=	ENSP00000330671.7:n.496-78C=
ENST00000409508.7:c.496-78C=	ENSP00000475939.1:n.496-78C=
ENST00000620169.4:c.496-78C=	ENSP00000481693.1:n.496-78C=
NM_001277115.1:c.496-78C=	NP_001264044.1:n.496-78C=
NM_001277115.2:c.496-78C= MANE Select	NP_001264044.1:n.496-78C=