Canonical Allele Identifier: CA366944415
Gene: DNAH11 HGNC NCBI

Linked Data

dbSNP Id: rs1785006812

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21599908T>A , CM000669.2:g.21599908T>A GRCh38
NC_000007.13:g.21639526T>A , CM000669.1:g.21639526T>A GRCh37
NC_000007.12:g.21606051T>A NCBI36
NG_012886.2:g.61694T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.2789T>A MANE Select ENSP00000475939.1:p.Phe930Tyr
ENST00000328843.10:c.2789T>A ENSP00000330671.7:p.Phe930Tyr
ENST00000409508.7:c.2789T>A ENSP00000475939.1:p.Phe930Tyr
ENST00000620169.4:c.2789T>A ENSP00000481693.1:p.Phe930Tyr
NM_001277115.1:c.2789T>A NP_001264044.1:p.Phe930Tyr
NM_001277115.2:c.2789T>A MANE Select NP_001264044.1:p.Phe930Tyr