Canonical Allele Identifier: CA366932681
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2817627
ClinVar RCV Id: RCV003650855
gnomAD v4: 7-21559000-T-C
COSMIC: COSM3880100 COSM3880101
MyVariant Identifiers: chr7:g.21598618T>C (hg19) chr7:g.21559000T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21559000T>C , CM000669.2:g.21559000T>C GRCh38
NC_000007.13:g.21598618T>C , CM000669.1:g.21598618T>C GRCh37
NC_000007.12:g.21565143T>C NCBI36
NG_012886.2:g.20786T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.692+2T>C MANE Select ENSP00000475939.1:n.692+2T>C
ENST00000328843.10:c.692+2T>C ENSP00000330671.7:n.692+2T>C
ENST00000409508.7:c.692+2T>C ENSP00000475939.1:n.692+2T>C
ENST00000620169.4:c.692+2T>C ENSP00000481693.1:n.692+2T>C
NM_001277115.1:c.692+2T>C NP_001264044.1:n.692+2T>C
NM_001277115.2:c.692+2T>C MANE Select NP_001264044.1:n.692+2T>C
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