Canonical Allele Identifier: CA155109155
Gene: DNAH11 HGNC NCBI

Linked Data

dbSNP Id: rs369204897
gnomAD v4: 7-21619196-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21619196G>A , CM000669.2:g.21619196G>A GRCh38
NC_000007.13:g.21658814G>A , CM000669.1:g.21658814G>A GRCh37
NC_000007.12:g.21625339G>A NCBI36
NG_012886.2:g.80982G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.4351G>A MANE Select ENSP00000475939.1:p.Ala1451Thr
ENST00000328843.10:c.4366G>A ENSP00000330671.7:p.Ala1456Thr
ENST00000409508.7:c.4351G>A ENSP00000475939.1:p.Ala1451Thr
ENST00000465593.1:n.377G>A
ENST00000620169.4:c.4366G>A ENSP00000481693.1:p.Ala1456Thr
NM_001277115.1:c.4351G>A NP_001264044.1:p.Ala1451Thr
NM_001277115.2:c.4351G>A MANE Select NP_001264044.1:p.Ala1451Thr