Canonical Allele Identifier: CA1693626933

Gene: DNAH11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21705667_21705668delinsTG , CM000669.2:g.21705667_21705668delinsTG	GRCh38
NC_000007.13:g.21745285_21745286delinsTG , CM000669.1:g.21745285_21745286delinsTG	GRCh37
NC_000007.12:g.21711810_21711811delinsTG	NCBI36
NG_012886.2:g.167453_167454delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.6546+130_6546+131delinsTG MANE Select	ENSP00000475939.1:n.6546+130_6546+131delinsTG
ENST00000328843.10:c.6567+130_6567+131delinsTG	ENSP00000330671.7:n.6567+130_6567+131delinsTG
ENST00000409508.7:c.6546+130_6546+131delinsTG	ENSP00000475939.1:n.6546+130_6546+131delinsTG
ENST00000620169.4:c.6567+130_6567+131delinsTG	ENSP00000481693.1:n.6567+130_6567+131delinsTG
NM_001277115.1:c.6546+130_6546+131delinsTG	NP_001264044.1:n.6546+130_6546+131delinsTG
NM_001277115.2:c.6546+130_6546+131delinsTG MANE Select	NP_001264044.1:n.6546+130_6546+131delinsTG