Canonical Allele Identifier: CA2681991203
Gene: DNAH11 HGNC NCBI

Linked Data

gnomAD v4: 7-21864475-TC-T
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21864477del , CM000669.2:g.21864477del GRCh38
NC_000007.13:g.21904095del , CM000669.1:g.21904095del GRCh37
NC_000007.12:g.21870620del NCBI36
NG_012886.2:g.326263del

Transcript Alleles

HGVS Amino-acid change
ENST00000409508.8:c.11374-58del MANE Select ENSP00000475939.1:n.11374-58del
ENST00000328843.10:c.11395-58del ENSP00000330671.7:n.11395-58del
ENST00000409508.7:c.11374-58del ENSP00000475939.1:n.11374-58del
ENST00000620169.4:c.11395-58del ENSP00000481693.1:n.11395-58del
NM_001277115.1:c.11374-58del NP_001264044.1:n.11374-58del
NM_001277115.2:c.11374-58del MANE Select NP_001264044.1:n.11374-58del
Search 100 bp 5'
Search 100 bp 3'