Canonical Allele Identifier: CA2681984322
Gene: DNAH11 HGNC NCBI

Linked Data

gnomAD v4: 7-21705568-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21705568A>T , CM000669.2:g.21705568A>T GRCh38
NC_000007.13:g.21745186A>T , CM000669.1:g.21745186A>T GRCh37
NC_000007.12:g.21711711A>T NCBI36
NG_012886.2:g.167354A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000409508.8:c.6546+31A>T MANE Select ENSP00000475939.1:n.6546+31A>T
ENST00000328843.10:c.6567+31A>T ENSP00000330671.7:n.6567+31A>T
ENST00000409508.7:c.6546+31A>T ENSP00000475939.1:n.6546+31A>T
ENST00000620169.4:c.6567+31A>T ENSP00000481693.1:n.6567+31A>T
NM_001277115.1:c.6546+31A>T NP_001264044.1:n.6546+31A>T
NM_001277115.2:c.6546+31A>T MANE Select NP_001264044.1:n.6546+31A>T
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