Canonical Allele Identifier: CA366943764
Gene: DNAH11 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.21639421T>A (hg19) chr7:g.21599803T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21599803T>A , CM000669.2:g.21599803T>A GRCh38
NC_000007.13:g.21639421T>A , CM000669.1:g.21639421T>A GRCh37
NC_000007.12:g.21605946T>A NCBI36
NG_012886.2:g.61589T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.2684T>A MANE Select ENSP00000475939.1:p.Phe895Tyr
ENST00000328843.10:c.2684T>A ENSP00000330671.7:p.Phe895Tyr
ENST00000409508.7:c.2684T>A ENSP00000475939.1:p.Phe895Tyr
ENST00000620169.4:c.2684T>A ENSP00000481693.1:p.Phe895Tyr
NM_001277115.1:c.2684T>A NP_001264044.1:p.Phe895Tyr
NM_001277115.2:c.2684T>A MANE Select NP_001264044.1:p.Phe895Tyr
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