Canonical Allele Identifier: CA155121362
Gene: DNAH11 HGNC NCBI

Linked Data

dbSNP Id: rs984400931

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21748687G>A , CM000669.2:g.21748687G>A GRCh38
NC_000007.13:g.21788305G>A , CM000669.1:g.21788305G>A GRCh37
NC_000007.12:g.21754830G>A NCBI36
NG_012886.2:g.210473G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.8618G>A MANE Select ENSP00000475939.1:p.Gly2873Asp
ENST00000328843.10:c.8639G>A ENSP00000330671.7:p.Gly2880Asp
ENST00000409508.7:c.8618G>A ENSP00000475939.1:p.Gly2873Asp
ENST00000620169.4:c.8639G>A ENSP00000481693.1:p.Gly2880Asp
NM_001277115.1:c.8618G>A NP_001264044.1:p.Gly2873Asp
NM_001277115.2:c.8618G>A MANE Select NP_001264044.1:p.Gly2873Asp