Canonical Allele Identifier: CA8951348
Gene: HAUS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.46125784G>A , CM000680.2:g.46125784G>A GRCh38
NC_000018.9:g.43705750G>A , CM000680.1:g.43705750G>A GRCh37
NC_000018.8:g.41959748G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000282058.11:c.779G>A MANE Select ENSP00000282058.5:p.Arg260Gln
ENST00000282058.10:c.779G>A ENSP00000282058.5:p.Arg260Gln
ENST00000585518.5:c.*12G>A ENSP00000467975.1:n.*12G>A
ENST00000586060.5:c.*157G>A ENSP00000466364.1:n.*157G>A
ENST00000588704.1:n.735G>A
ENST00000589554.5:c.*223G>A ENSP00000466715.1:n.*223G>A
ENST00000591715.5:c.*576G>A ENSP00000465093.1:n.*576G>A
ENST00000593165.5:c.907G>A
ENST00000595199.1:n.225G>A
NM_138443.3:c.779G>A NP_612452.1:p.Arg260Gln
NR_026978.1:n.899G>A
NM_138443.4:c.779G>A MANE Select NP_612452.1:p.Arg260Gln
NR_026978.2:n.846G>A