Canonical Allele Identifier: CA366952529
Gene: DNAH11 HGNC NCBI

Linked Data

dbSNP Id: rs2128453725

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21619119A>T , CM000669.2:g.21619119A>T GRCh38
NC_000007.13:g.21658737A>T , CM000669.1:g.21658737A>T GRCh37
NC_000007.12:g.21625262A>T NCBI36
NG_012886.2:g.80905A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.4274A>T MANE Select ENSP00000475939.1:p.Glu1425Val
ENST00000328843.10:c.4289A>T ENSP00000330671.7:p.Glu1430Val
ENST00000409508.7:c.4274A>T ENSP00000475939.1:p.Glu1425Val
ENST00000465593.1:n.300A>T
ENST00000620169.4:c.4289A>T ENSP00000481693.1:p.Glu1430Val
NM_001277115.1:c.4274A>T NP_001264044.1:p.Glu1425Val
NM_001277115.2:c.4274A>T MANE Select NP_001264044.1:p.Glu1425Val