Canonical Allele Identifier: CA1693722257

Gene: DNAH11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21864505_21864507delinsTAA , CM000669.2:g.21864505_21864507delinsTAA	GRCh38
NC_000007.13:g.21904123_21904125delinsTAA , CM000669.1:g.21904123_21904125delinsTAA	GRCh37
NC_000007.12:g.21870648_21870650delinsTAA	NCBI36
NG_012886.2:g.326291_326293delinsTAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.11374-30_11374-28delinsTAA MANE Select	ENSP00000475939.1:n.11374-30_11374-28delinsTAA
ENST00000328843.10:c.11395-30_11395-28delinsTAA	ENSP00000330671.7:n.11395-30_11395-28delinsTAA
ENST00000409508.7:c.11374-30_11374-28delinsTAA	ENSP00000475939.1:n.11374-30_11374-28delinsTAA
ENST00000620169.4:c.11395-30_11395-28delinsTAA	ENSP00000481693.1:n.11395-30_11395-28delinsTAA
NM_001277115.1:c.11374-30_11374-28delinsTAA	NP_001264044.1:n.11374-30_11374-28delinsTAA
NM_001277115.2:c.11374-30_11374-28delinsTAA MANE Select	NP_001264044.1:n.11374-30_11374-28delinsTAA