Canonical Allele Identifier: CA2739266282
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2818491
ClinVar RCV Id: RCV003650873
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21880696del , CM000669.2:g.21880696del GRCh38
NC_000007.13:g.21920314del , CM000669.1:g.21920314del GRCh37
NC_000007.12:g.21886839del NCBI36
NG_012886.2:g.342482del

Transcript Alleles

HGVS Amino-acid change
ENST00000409508.8:c.12196-6del MANE Select ENSP00000475939.1:n.12196-6del
ENST00000328843.10:c.12217-6del ENSP00000330671.7:n.12217-6del
ENST00000409508.7:c.12196-6del ENSP00000475939.1:n.12196-6del
ENST00000620169.4:c.12217-6del ENSP00000481693.1:n.12217-6del
NM_001277115.1:c.12196-6del NP_001264044.1:n.12196-6del
NM_001277115.2:c.12196-6del MANE Select NP_001264044.1:n.12196-6del
Search 100 bp 5'
Search 100 bp 3'