Canonical Allele Identifier: CA2834860034
Gene: DNAH11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21816956del , CM000669.2:g.21816956del GRCh38
NC_000007.13:g.21856574del , CM000669.1:g.21856574del GRCh37
NC_000007.12:g.21823099del NCBI36
NG_012886.2:g.278742del

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.10568+254del MANE Select ENSP00000475939.1:n.10568+254del
ENST00000328843.10:c.10589+254del ENSP00000330671.7:n.10589+254del
ENST00000409508.7:c.10568+254del ENSP00000475939.1:n.10568+254del
ENST00000620169.4:c.10589+254del ENSP00000481693.1:n.10589+254del
NM_001277115.1:c.10568+254del NP_001264044.1:n.10568+254del
NM_001277115.2:c.10568+254del MANE Select NP_001264044.1:n.10568+254del