Canonical Allele Identifier: CA2681979583
Gene: DNAH11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21600211del , CM000669.2:g.21600211del GRCh38
NC_000007.13:g.21639829del , CM000669.1:g.21639829del GRCh37
NC_000007.12:g.21606354del NCBI36
NG_012886.2:g.61997del

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.3000+92del MANE Select ENSP00000475939.1:n.3000+92del
ENST00000328843.10:c.3000+92del ENSP00000330671.7:n.3000+92del
ENST00000409508.7:c.3000+92del ENSP00000475939.1:n.3000+92del
ENST00000620169.4:c.3000+92del ENSP00000481693.1:n.3000+92del
NM_001277115.1:c.3000+92del NP_001264044.1:n.3000+92del
NM_001277115.2:c.3000+92del MANE Select NP_001264044.1:n.3000+92del