Canonical Allele Identifier: CA1693579785
Gene: DNAH11 HGNC NCBI

Linked Data

dbSNP Id: rs1785025460
gnomAD v4: 7-21600254-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21600254G>A , CM000669.2:g.21600254G>A GRCh38
NC_000007.13:g.21639872G>A , CM000669.1:g.21639872G>A GRCh37
NC_000007.12:g.21606397G>A NCBI36
NG_012886.2:g.62040G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.3000+135G>A MANE Select ENSP00000475939.1:n.3000+135G>A
ENST00000328843.10:c.3000+135G>A ENSP00000330671.7:n.3000+135G>A
ENST00000409508.7:c.3000+135G>A ENSP00000475939.1:n.3000+135G>A
ENST00000620169.4:c.3000+135G>A ENSP00000481693.1:n.3000+135G>A
NM_001277115.1:c.3000+135G>A NP_001264044.1:n.3000+135G>A
NM_001277115.2:c.3000+135G>A MANE Select NP_001264044.1:n.3000+135G>A
Search 100 bp 5'
Search 100 bp 3'