Canonical Allele Identifier: CA15921731
Gene: HAUS1 HGNC NCBI

Linked Data

dbSNP Id: rs11874712

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.46108610C>A , CM000680.2:g.46108610C>A GRCh38
NC_000018.9:g.43688576C>A , CM000680.1:g.43688576C>A GRCh37
NC_000018.8:g.41942574C>A NCBI36
NG_041769.1:g.624G>T
NG_041769.2:g.5624G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000282058.11:c.205+3242C>A MANE Select ENSP00000282058.5:n.205+3242C>A
ENST00000282058.10:c.205+3242C>A ENSP00000282058.5:n.205+3242C>A
ENST00000585518.5:c.205+3242C>A ENSP00000467975.1:n.205+3242C>A
ENST00000586060.5:c.205+3242C>A ENSP00000466364.1:n.205+3242C>A
ENST00000589554.5:c.205+3242C>A ENSP00000466715.1:n.205+3242C>A
ENST00000591098.1:n.237+3242C>A
ENST00000591715.5:c.*2+3202C>A ENSP00000465093.1:n.*2+3202C>A
ENST00000592206.5:c.*118+1777C>A ENSP00000465492.1:n.*118+1777C>A
ENST00000592471.1:c.151+3242C>A ENSP00000468575.1:n.151+3242C>A
ENST00000593165.5:c.196-1037C>A
NM_138443.3:c.205+3242C>A NP_612452.1:n.205+3242C>A
NR_026978.1:n.325+3202C>A
NM_138443.4:c.205+3242C>A MANE Select NP_612452.1:n.205+3242C>A
NR_026978.2:n.272+3202C>A