Canonical Allele Identifier: CA2142596605
Gene: ESR2 HGNC NCBI

Linked Data

dbSNP Id: rs2076909703

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.64293821_64293822del , CM000676.2:g.64293821_64293822del GRCh38
NC_000014.8:g.64760539_64760540del , CM000676.1:g.64760539_64760540del GRCh37
NC_000014.7:g.63830292_63830293del NCBI36
NG_011535.1:g.49729_49730del

Transcript Alleles

HGVS Amino-acid Change
ENST00000341099.6:c.-91+211_-91+212del MANE Select ENSP00000343925.4:n.-91+211_-91+212del
ENST00000341099.5:c.-91+211_-91+212del ENSP00000343925.4:n.-91+211_-91+212del
ENST00000353772.7:c.-91+211_-91+212del ENSP00000335551.4:n.-91+211_-91+212del
ENST00000358599.9:c.-90-10747_-90-10746del ENSP00000351412.5:n.-90-10747_-90-10746del
ENST00000554572.5:c.-91+3711_-91+3712del ENSP00000450699.1:n.-91+3711_-91+3712del
ENST00000556275.5:c.-91+211_-91+212del ENSP00000452485.2:n.-91+211_-91+212del
NM_001040275.1:c.-91+211_-91+212del NP_001035365.1:n.-91+211_-91+212del
NM_001291712.1:c.-91+3711_-91+3712del NP_001278641.1:n.-91+3711_-91+3712del
NM_001291723.1:c.-90-10747_-90-10746del NP_001278652.1:n.-90-10747_-90-10746del
NM_001437.2:c.-91+211_-91+212del NP_001428.1:n.-91+211_-91+212del
NR_073496.1:n.654-10747_654-10746del
XM_011536545.1:c.-91+211_-91+212del XP_011534847.1:n.-91+211_-91+212del
XM_011536546.1:c.-91+7546_-91+7547del XP_011534848.1:n.-91+7546_-91+7547del
XM_017021079.1:c.-90-10747_-90-10746del XP_016876568.1:n.-90-10747_-90-10746del
XM_017021080.1:c.-90-10747_-90-10746del XP_016876569.1:n.-90-10747_-90-10746del
XM_017021081.1:c.-90-10747_-90-10746del XP_016876570.1:n.-90-10747_-90-10746del
XM_017021082.1:c.-90-10747_-90-10746del XP_016876571.1:n.-90-10747_-90-10746del
XM_017021083.1:c.-90-10747_-90-10746del XP_016876572.1:n.-90-10747_-90-10746del
XM_017021084.1:c.-90-10747_-90-10746del XP_016876573.1:n.-90-10747_-90-10746del
XR_001750187.1:n.485+211_485+212del
NM_001291712.2:c.-91+3711_-91+3712del NP_001278641.1:n.-91+3711_-91+3712del
NR_073496.2:n.717-10747_717-10746del
NM_001437.3:c.-91+211_-91+212del MANE Select NP_001428.1:n.-91+211_-91+212del