Canonical Allele Identifier: CA454139675
Gene: DNAH11 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.21675659A>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21636041A>C , CM000669.2:g.21636041A>C GRCh38
NC_000007.13:g.21675659A>C , CM000669.1:g.21675659A>C GRCh37
NC_000007.12:g.21642184A>C NCBI36
NG_012886.2:g.97827A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.4671A>C MANE Select ENSP00000475939.1:p.Arg1557=
ENST00000328843.10:c.4686A>C ENSP00000330671.7:p.Arg1562=
ENST00000409508.7:c.4671A>C ENSP00000475939.1:p.Arg1557=
ENST00000465593.1:n.697A>C
ENST00000620169.4:c.4686A>C ENSP00000481693.1:p.Arg1562=
NM_001277115.1:c.4671A>C NP_001264044.1:p.Arg1557=
NM_001277115.2:c.4671A>C MANE Select NP_001264044.1:p.Arg1557=
Search 100 bp 5'
Search 100 bp 3'