Canonical Allele Identifier: CA2681984261
Gene: DNAH11 HGNC NCBI

Linked Data

gnomAD v4: 7-21705352-TG-T
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21705357del , CM000669.2:g.21705357del GRCh38
NC_000007.13:g.21744975del , CM000669.1:g.21744975del GRCh37
NC_000007.12:g.21711500del NCBI36
NG_012886.2:g.167143del

Transcript Alleles

HGVS Amino-acid change
ENST00000409508.8:c.6469-103del MANE Select ENSP00000475939.1:n.6469-103del
ENST00000328843.10:c.6490-103del ENSP00000330671.7:n.6490-103del
ENST00000409508.7:c.6469-103del ENSP00000475939.1:n.6469-103del
ENST00000620169.4:c.6490-103del ENSP00000481693.1:n.6490-103del
NM_001277115.1:c.6469-103del NP_001264044.1:n.6469-103del
NM_001277115.2:c.6469-103del MANE Select NP_001264044.1:n.6469-103del
Search 100 bp 5'
Search 100 bp 3'