Canonical Allele Identifier: CA147209
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 93687
dbSNP Id: rs57208694

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21619237A>G , CM000669.2:g.21619237A>G GRCh38
NC_000007.13:g.21658855A>G , CM000669.1:g.21658855A>G GRCh37
NC_000007.12:g.21625380A>G NCBI36
NG_012886.2:g.81023A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000409508.8:c.4377+15A>G MANE Select ENSP00000475939.1:p.=
ENST00000328843.10:c.4392+15A>G ENSP00000330671.7:p.=
ENST00000409508.7:c.4377+15A>G ENSP00000475939.1:p.=
ENST00000465593.1:n.403+15A>G
ENST00000620169.4:c.4392+15A>G ENSP00000481693.1:p.=
NM_001277115.1:c.4377+15A>G NP_001264044.1:p.=
NM_001277115.2:c.4377+15A>G MANE Select NP_001264044.1:p.=