Canonical Allele Identifier: CA366955787
Gene: DNAH11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21749724C>G , CM000669.2:g.21749724C>G GRCh38
NC_000007.13:g.21789342C>G , CM000669.1:g.21789342C>G GRCh37
NC_000007.12:g.21755867C>G NCBI36
NG_012886.2:g.211510C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.8720C>G MANE Select ENSP00000475939.1:p.Pro2907Arg
ENST00000328843.10:c.8741C>G ENSP00000330671.7:p.Pro2914Arg
ENST00000409508.7:c.8720C>G ENSP00000475939.1:p.Pro2907Arg
ENST00000620169.4:c.8741C>G ENSP00000481693.1:p.Pro2914Arg
NM_001277115.1:c.8720C>G NP_001264044.1:p.Pro2907Arg
NM_001277115.2:c.8720C>G MANE Select NP_001264044.1:p.Pro2907Arg