Canonical Allele Identifier: CA1099224130
Gene: DNAH11 HGNC NCBI

Linked Data

dbSNP Id: rs1783334012
gnomAD v3: 7-21559001-A-AC
gnomAD v4: 7-21559001-A-AC
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21559002dup , CM000669.2:g.21559002dup GRCh38
NC_000007.13:g.21598620dup , CM000669.1:g.21598620dup GRCh37
NC_000007.12:g.21565145dup NCBI36
NG_012886.2:g.20788dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.692+4dup MANE Select ENSP00000475939.1:n.692+4dup
ENST00000328843.10:c.692+4dup ENSP00000330671.7:n.692+4dup
ENST00000409508.7:c.692+4dup ENSP00000475939.1:n.692+4dup
ENST00000620169.4:c.692+4dup ENSP00000481693.1:n.692+4dup
NM_001277115.1:c.692+4dup NP_001264044.1:n.692+4dup
NM_001277115.2:c.692+4dup MANE Select NP_001264044.1:n.692+4dup
Search 100 bp 5'
Search 100 bp 3'