Canonical Allele Identifier: CA2681984248
Gene: DNAH11 HGNC NCBI

Linked Data

gnomAD v4: 7-21705342-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21705342C>T , CM000669.2:g.21705342C>T GRCh38
NC_000007.13:g.21744960C>T , CM000669.1:g.21744960C>T GRCh37
NC_000007.12:g.21711485C>T NCBI36
NG_012886.2:g.167128C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.6469-118C>T MANE Select ENSP00000475939.1:n.6469-118C>T
ENST00000328843.10:c.6490-118C>T ENSP00000330671.7:n.6490-118C>T
ENST00000409508.7:c.6469-118C>T ENSP00000475939.1:n.6469-118C>T
ENST00000620169.4:c.6490-118C>T ENSP00000481693.1:n.6490-118C>T
NM_001277115.1:c.6469-118C>T NP_001264044.1:n.6469-118C>T
NM_001277115.2:c.6469-118C>T MANE Select NP_001264044.1:n.6469-118C>T
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