Canonical Allele Identifier: CA1693708987

Gene: DNAH11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21854375G= , CM000669.2:g.21854375G=	GRCh38
NC_000007.13:g.21893993G= , CM000669.1:g.21893993G=	GRCh37
NC_000007.12:g.21860518G=	NCBI36
NG_012886.2:g.316161G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000409508.8:c.11122G= MANE Select	ENSP00000475939.1:p.Val3708=
ENST00000328843.10:c.11143G=	ENSP00000330671.7:p.Val3715=
ENST00000409508.7:c.11122G=	ENSP00000475939.1:p.Val3708=
ENST00000421290.1:n.305G=
ENST00000607413.5:n.385G=
ENST00000620169.4:c.11143G=	ENSP00000481693.1:p.Val3715=
NM_001277115.1:c.11122G=	NP_001264044.1:p.Val3708=
NM_001277115.2:c.11122G= MANE Select	NP_001264044.1:p.Val3708=