Canonical Allele Identifier: CA1099221376
Gene: DNAH11 HGNC NCBI

Linked Data

gnomAD v3: 7-21705688-T-TC
gnomAD v4: 7-21705688-T-TC
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21705688_21705689insC , CM000669.2:g.21705688_21705689insC GRCh38
NC_000007.13:g.21745306_21745307insC , CM000669.1:g.21745306_21745307insC GRCh37
NC_000007.12:g.21711831_21711832insC NCBI36
NG_012886.2:g.167474_167475insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.6546+151_6546+152insC MANE Select ENSP00000475939.1:n.6546+151_6546+152insC
ENST00000328843.10:c.6567+151_6567+152insC ENSP00000330671.7:n.6567+151_6567+152insC
ENST00000409508.7:c.6546+151_6546+152insC ENSP00000475939.1:n.6546+151_6546+152insC
ENST00000620169.4:c.6567+151_6567+152insC ENSP00000481693.1:n.6567+151_6567+152insC
NM_001277115.1:c.6546+151_6546+152insC NP_001264044.1:n.6546+151_6546+152insC
NM_001277115.2:c.6546+151_6546+152insC MANE Select NP_001264044.1:n.6546+151_6546+152insC
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