Canonical Allele Identifier: CA1099205695
Gene: DNAH11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21567635_21567643del , CM000669.2:g.21567635_21567643del GRCh38
NC_000007.13:g.21607253_21607261del , CM000669.1:g.21607253_21607261del GRCh37
NC_000007.12:g.21573778_21573786del NCBI36
NG_012886.2:g.29421_29429del

Transcript Alleles

HGVS Amino-acid change
ENST00000409508.8:c.1195-2434_1195-2426del MANE Select ENSP00000475939.1:n.1195-2434_1195-2426de...
ENST00000328843.10:c.1195-2434_1195-2426del ENSP00000330671.7:n.1195-2434_1195-2426de...
ENST00000409508.7:c.1195-2434_1195-2426del ENSP00000475939.1:n.1195-2434_1195-2426de...
ENST00000496218.1:n.81-2434_81-2426del
ENST00000620169.4:c.1195-2434_1195-2426del ENSP00000481693.1:n.1195-2434_1195-2426de...
NM_001277115.1:c.1195-2434_1195-2426del NP_001264044.1:n.1195-2434_1195-2426del
XR_927090.1:n.563+5683_563+5691del
XR_001745114.1:n.2793+5683_2793+5691del
NM_001277115.2:c.1195-2434_1195-2426del MANE Select NP_001264044.1:n.1195-2434_1195-2426del