Canonical Allele Identifier: CA2739266275
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2834138
ClinVar RCV Id: RCV003651250
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21748566del , CM000669.2:g.21748566del GRCh38
NC_000007.13:g.21788184del , CM000669.1:g.21788184del GRCh37
NC_000007.12:g.21754709del NCBI36
NG_012886.2:g.210352del

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.8511-14del MANE Select ENSP00000475939.1:n.8511-14del
ENST00000328843.10:c.8532-14del ENSP00000330671.7:n.8532-14del
ENST00000409508.7:c.8511-14del ENSP00000475939.1:n.8511-14del
ENST00000620169.4:c.8532-14del ENSP00000481693.1:n.8532-14del
NM_001277115.1:c.8511-14del NP_001264044.1:n.8511-14del
NM_001277115.2:c.8511-14del MANE Select NP_001264044.1:n.8511-14del
Search 100 bp 5'
Search 100 bp 3'