Canonical Allele Identifier: CA2681984291
Gene: DNAH11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21705414_21705420del , CM000669.2:g.21705414_21705420del GRCh38
NC_000007.13:g.21745032_21745038del , CM000669.1:g.21745032_21745038del GRCh37
NC_000007.12:g.21711557_21711563del NCBI36
NG_012886.2:g.167200_167206del

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.6469-46_6469-40del MANE Select ENSP00000475939.1:n.6469-46_6469-40del
ENST00000328843.10:c.6490-46_6490-40del ENSP00000330671.7:n.6490-46_6490-40del
ENST00000409508.7:c.6469-46_6469-40del ENSP00000475939.1:n.6469-46_6469-40del
ENST00000620169.4:c.6490-46_6490-40del ENSP00000481693.1:n.6490-46_6490-40del
NM_001277115.1:c.6469-46_6469-40del NP_001264044.1:n.6469-46_6469-40del
NM_001277115.2:c.6469-46_6469-40del MANE Select NP_001264044.1:n.6469-46_6469-40del