Canonical Allele Identifier: CA366933670
Gene: DNAH11 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.21675682G>T (hg19) chr7:g.21636064G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21636064G>T , CM000669.2:g.21636064G>T GRCh38
NC_000007.13:g.21675682G>T , CM000669.1:g.21675682G>T GRCh37
NC_000007.12:g.21642207G>T NCBI36
NG_012886.2:g.97850G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.4694G>T MANE Select ENSP00000475939.1:p.Arg1565Ile
ENST00000328843.10:c.4709G>T ENSP00000330671.7:p.Arg1570Ile
ENST00000409508.7:c.4694G>T ENSP00000475939.1:p.Arg1565Ile
ENST00000465593.1:n.720G>T
ENST00000620169.4:c.4709G>T ENSP00000481693.1:p.Arg1570Ile
NM_001277115.1:c.4694G>T NP_001264044.1:p.Arg1565Ile
NM_001277115.2:c.4694G>T MANE Select NP_001264044.1:p.Arg1565Ile
Search 100 bp 5'
Search 100 bp 3'