Canonical Allele Identifier: CA2774675051
Gene: DNAH11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21600200del , CM000669.2:g.21600200del GRCh38
NC_000007.13:g.21639818del , CM000669.1:g.21639818del GRCh37
NC_000007.12:g.21606343del NCBI36
NG_012886.2:g.61986del

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.3000+81del MANE Select ENSP00000475939.1:n.3000+81del
ENST00000328843.10:c.3000+81del ENSP00000330671.7:n.3000+81del
ENST00000409508.7:c.3000+81del ENSP00000475939.1:n.3000+81del
ENST00000620169.4:c.3000+81del ENSP00000481693.1:n.3000+81del
NM_001277115.1:c.3000+81del NP_001264044.1:n.3000+81del
NM_001277115.2:c.3000+81del MANE Select NP_001264044.1:n.3000+81del