Canonical Allele Identifier: CA366938021
Gene: DNAH11 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.21745082T>A (hg19) chr7:g.21705464T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21705464T>A , CM000669.2:g.21705464T>A GRCh38
NC_000007.13:g.21745082T>A , CM000669.1:g.21745082T>A GRCh37
NC_000007.12:g.21711607T>A NCBI36
NG_012886.2:g.167250T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.6473T>A MANE Select ENSP00000475939.1:p.Val2158Asp
ENST00000328843.10:c.6494T>A ENSP00000330671.7:p.Val2165Asp
ENST00000409508.7:c.6473T>A ENSP00000475939.1:p.Val2158Asp
ENST00000620169.4:c.6494T>A ENSP00000481693.1:p.Val2165Asp
NM_001277115.1:c.6473T>A NP_001264044.1:p.Val2158Asp
NM_001277115.2:c.6473T>A MANE Select NP_001264044.1:p.Val2158Asp
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