Canonical Allele Identifier: CA366952650
Gene: DNAH11 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.21658802A>T (hg19) chr7:g.21619184A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21619184A>T , CM000669.2:g.21619184A>T GRCh38
NC_000007.13:g.21658802A>T , CM000669.1:g.21658802A>T GRCh37
NC_000007.12:g.21625327A>T NCBI36
NG_012886.2:g.80970A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.4339A>T MANE Select ENSP00000475939.1:p.Ile1447Phe
ENST00000328843.10:c.4354A>T ENSP00000330671.7:p.Ile1452Phe
ENST00000409508.7:c.4339A>T ENSP00000475939.1:p.Ile1447Phe
ENST00000465593.1:n.365A>T
ENST00000620169.4:c.4354A>T ENSP00000481693.1:p.Ile1452Phe
NM_001277115.1:c.4339A>T NP_001264044.1:p.Ile1447Phe
NM_001277115.2:c.4339A>T MANE Select NP_001264044.1:p.Ile1447Phe
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