Canonical Allele Identifier: CA366952488
Gene: DNAH11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21619103A>G , CM000669.2:g.21619103A>G GRCh38
NC_000007.13:g.21658721A>G , CM000669.1:g.21658721A>G GRCh37
NC_000007.12:g.21625246A>G NCBI36
NG_012886.2:g.80889A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.4258A>G MANE Select ENSP00000475939.1:p.Lys1420Glu
ENST00000328843.10:c.4273A>G ENSP00000330671.7:p.Lys1425Glu
ENST00000409508.7:c.4258A>G ENSP00000475939.1:p.Lys1420Glu
ENST00000465593.1:n.284A>G
ENST00000620169.4:c.4273A>G ENSP00000481693.1:p.Lys1425Glu
NM_001277115.1:c.4258A>G NP_001264044.1:p.Lys1420Glu
NM_001277115.2:c.4258A>G MANE Select NP_001264044.1:p.Lys1420Glu