Canonical Allele Identifier: CA1099223968
Gene: DNAH11 HGNC NCBI

Linked Data

dbSNP Id: rs1783318184
gnomAD v3: 7-21558691-A-AT
gnomAD v4: 7-21558691-A-AT
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21558693dup , CM000669.2:g.21558693dup GRCh38
NC_000007.13:g.21598311dup , CM000669.1:g.21598311dup GRCh37
NC_000007.12:g.21564836dup NCBI36
NG_012886.2:g.20479dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.496-109dup MANE Select ENSP00000475939.1:n.496-109dup
ENST00000328843.10:c.496-109dup ENSP00000330671.7:n.496-109dup
ENST00000409508.7:c.496-109dup ENSP00000475939.1:n.496-109dup
ENST00000620169.4:c.496-109dup ENSP00000481693.1:n.496-109dup
NM_001277115.1:c.496-109dup NP_001264044.1:n.496-109dup
NM_001277115.2:c.496-109dup MANE Select NP_001264044.1:n.496-109dup
Search 100 bp 5'
Search 100 bp 3'