Canonical Allele Identifier: CA2774673628
Gene: DNAH11 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21543431del , CM000669.2:g.21543431del GRCh38
NC_000007.13:g.21583049del , CM000669.1:g.21583049del GRCh37
NC_000007.12:g.21549574del NCBI36
NG_012886.2:g.5217del

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.186del MANE Select ENSP00000475939.1:p.Gly63AlafsTer6
ENST00000328843.10:c.186del ENSP00000330671.7:p.Gly63AlafsTer6
ENST00000409508.7:c.186del ENSP00000475939.1:p.Gly63AlafsTer6
ENST00000620169.4:c.186del ENSP00000481693.1:p.Gly63AlafsTer6
NM_001277115.1:c.186del NP_001264044.1:p.Gly63AlafsTer6
NM_001277115.2:c.186del MANE Select NP_001264044.1:p.Gly63AlafsTer6
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Search 100 bp 3'