Canonical Allele Identifier: CA2774675567
Gene: DNAH11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21619089_21619098del , CM000669.2:g.21619089_21619098del GRCh38
NC_000007.13:g.21658707_21658716del , CM000669.1:g.21658707_21658716del GRCh37
NC_000007.12:g.21625232_21625241del NCBI36
NG_012886.2:g.80875_80884del

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.4255-11_4255-2del MANE Select ENSP00000475939.1:n.4255-11_4255-2del
ENST00000328843.10:c.4270-11_4270-2del ENSP00000330671.7:n.4270-11_4270-2del
ENST00000409508.7:c.4255-11_4255-2del ENSP00000475939.1:n.4255-11_4255-2del
ENST00000465593.1:n.281-11_281-2del
ENST00000620169.4:c.4270-11_4270-2del ENSP00000481693.1:n.4270-11_4270-2del
NM_001277115.1:c.4255-11_4255-2del NP_001264044.1:n.4255-11_4255-2del
NM_001277115.2:c.4255-11_4255-2del MANE Select NP_001264044.1:n.4255-11_4255-2del