Canonical Allele Identifier: CA1693661595
Gene: DNAH11 HGNC NCBI

Linked Data

dbSNP Id: rs1786251660
gnomAD v4: 7-21748442-T-TCGA
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21748444_21748445insACG , CM000669.2:g.21748444_21748445insACG GRCh38
NC_000007.13:g.21788062_21788063insACG , CM000669.1:g.21788062_21788063insACG GRCh37
NC_000007.12:g.21754587_21754588insACG NCBI36
NG_012886.2:g.210230_210231insACG

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.8511-136_8511-135insACG MANE Select ENSP00000475939.1:n.8511-136_8511-135insACG
ENST00000328843.10:c.8532-136_8532-135insACG ENSP00000330671.7:n.8532-136_8532-135insACG
ENST00000409508.7:c.8511-136_8511-135insACG ENSP00000475939.1:n.8511-136_8511-135insACG
ENST00000620169.4:c.8532-136_8532-135insACG ENSP00000481693.1:n.8532-136_8532-135insACG
NM_001277115.1:c.8511-136_8511-135insACG NP_001264044.1:n.8511-136_8511-135insACG
NM_001277115.2:c.8511-136_8511-135insACG MANE Select NP_001264044.1:n.8511-136_8511-135insACG
Search 100 bp 5'
Search 100 bp 3'