Canonical Allele Identifier: CA366949069
Gene: DNAH11 HGNC NCBI

Linked Data

dbSNP Id: rs1789808097
gnomAD v4: 7-21816663-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21816663A>G , CM000669.2:g.21816663A>G GRCh38
NC_000007.13:g.21856281A>G , CM000669.1:g.21856281A>G GRCh37
NC_000007.12:g.21822806A>G NCBI36
NG_012886.2:g.278449A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.10529A>G MANE Select ENSP00000475939.1:p.Tyr3510Cys
ENST00000328843.10:c.10550A>G ENSP00000330671.7:p.Tyr3517Cys
ENST00000409508.7:c.10529A>G ENSP00000475939.1:p.Tyr3510Cys
ENST00000620169.4:c.10550A>G ENSP00000481693.1:p.Tyr3517Cys
NM_001277115.1:c.10529A>G NP_001264044.1:p.Tyr3510Cys
NM_001277115.2:c.10529A>G MANE Select NP_001264044.1:p.Tyr3510Cys