Canonical Allele Identifier: CA402364704
Community Standard Title: NM_138443.4(HAUS1):c.399T>G (p.Ser133Arg)
Gene: HAUS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.46119983T>G , CM000680.2:g.46119983T>G GRCh38
NC_000018.9:g.43699949T>G , CM000680.1:g.43699949T>G GRCh37
NC_000018.8:g.41953947T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_138443.4:c.399T>G MANE Select NP_612452.1:p.Ser133Arg
ENST00000282058.11:c.399T>G MANE Select ENSP00000282058.5:p.Ser133Arg
NM_138443.3:c.399T>G NP_612452.1:p.Ser133Arg
NR_026978.1:n.519T>G
NR_026978.2:n.466T>G
ENST00000282058.10:c.399T>G ENSP00000282058.5:p.Ser133Arg
ENST00000585518.5:c.206-3316T>G ENSP00000467975.1:n.206-3316T>G
ENST00000586060.5:c.206-2484T>G ENSP00000466364.1:n.206-2484T>G
ENST00000588704.1:n.355T>G
ENST00000589554.5:c.206-2484T>G ENSP00000466715.1:n.206-2484T>G
ENST00000591715.5:c.*196T>G ENSP00000465093.1:n.*196T>G
ENST00000592206.5:c.*312T>G ENSP00000465492.1:n.*312T>G
ENST00000593165.5:c.527T>G