Canonical Allele Identifier: CA2551583832
Gene: DNAH11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21880964del , CM000669.2:g.21880964del GRCh38
NC_000007.13:g.21920582del , CM000669.1:g.21920582del GRCh37
NC_000007.12:g.21887107del NCBI36
NG_012886.2:g.342750del

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.12387+71del MANE Select ENSP00000475939.1:n.12387+71del
ENST00000328843.10:c.12408+71del ENSP00000330671.7:n.12408+71del
ENST00000409508.7:c.12387+71del ENSP00000475939.1:n.12387+71del
ENST00000620169.4:c.12408+71del ENSP00000481693.1:n.12408+71del
NM_001277115.1:c.12387+71del NP_001264044.1:n.12387+71del
NM_001277115.2:c.12387+71del MANE Select NP_001264044.1:n.12387+71del