Canonical Allele Identifier: CA366952579
Gene: DNAH11 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.21658766C>G (hg19) chr7:g.21619148C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21619148C>G , CM000669.2:g.21619148C>G GRCh38
NC_000007.13:g.21658766C>G , CM000669.1:g.21658766C>G GRCh37
NC_000007.12:g.21625291C>G NCBI36
NG_012886.2:g.80934C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.4303C>G MANE Select ENSP00000475939.1:p.Leu1435Val
ENST00000328843.10:c.4318C>G ENSP00000330671.7:p.Leu1440Val
ENST00000409508.7:c.4303C>G ENSP00000475939.1:p.Leu1435Val
ENST00000465593.1:n.329C>G
ENST00000620169.4:c.4318C>G ENSP00000481693.1:p.Leu1440Val
NM_001277115.1:c.4303C>G NP_001264044.1:p.Leu1435Val
NM_001277115.2:c.4303C>G MANE Select NP_001264044.1:p.Leu1435Val
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