Canonical Allele Identifier: CA273322011
Gene: REC114 HGNC NCBI

Linked Data

dbSNP Id: rs11635553

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73457267G>A , CM000677.2:g.73457267G>A GRCh38
NC_000015.9:g.73749608G>A , CM000677.1:g.73749608G>A GRCh37
NC_000015.8:g.71536661G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000331090.11:c.159+13923G>A MANE Select ENSP00000328423.6:n.159+13923G>A
ENST00000331090.10:c.159+13923G>A ENSP00000328423.6:n.159+13923G>A
ENST00000560581.1:c.159+13923G>A ENSP00000452908.1:n.159+13923G>A
NM_001042367.1:c.159+13923G>A NP_001035826.1:n.159+13923G>A
XM_011521461.1:c.244-16565G>A XP_011519763.1:n.244-16565G>A
XM_011521462.1:c.244-16565G>A XP_011519764.1:n.244-16565G>A
NM_001348772.1:c.159+13923G>A NP_001335701.1:n.159+13923G>A
NM_001042367.2:c.159+13923G>A MANE Select NP_001035826.1:n.159+13923G>A
NM_001348772.2:c.159+13923G>A NP_001335701.1:n.159+13923G>A