Canonical Allele Identifier: CA707700751
Gene: ESR2 HGNC NCBI

Linked Data

dbSNP Id: rs1352407267

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.64293787_64293794del , CM000676.2:g.64293787_64293794del GRCh38
NC_000014.8:g.64760505_64760512del , CM000676.1:g.64760505_64760512del GRCh37
NC_000014.7:g.63830258_63830265del NCBI36
NG_011535.1:g.49761_49768del

Transcript Alleles

HGVS Amino-acid Change
ENST00000341099.6:c.-91+243_-91+250del MANE Select ENSP00000343925.4:n.-91+243_-91+250del
ENST00000341099.5:c.-91+243_-91+250del ENSP00000343925.4:n.-91+243_-91+250del
ENST00000353772.7:c.-91+243_-91+250del ENSP00000335551.4:n.-91+243_-91+250del
ENST00000358599.9:c.-90-10715_-90-10708del ENSP00000351412.5:n.-90-10715_-90-10708del
ENST00000554572.5:c.-91+3743_-91+3750del ENSP00000450699.1:n.-91+3743_-91+3750del
ENST00000556275.5:c.-91+243_-91+250del ENSP00000452485.2:n.-91+243_-91+250del
NM_001040275.1:c.-91+243_-91+250del NP_001035365.1:n.-91+243_-91+250del
NM_001291712.1:c.-91+3743_-91+3750del NP_001278641.1:n.-91+3743_-91+3750del
NM_001291723.1:c.-90-10715_-90-10708del NP_001278652.1:n.-90-10715_-90-10708del
NM_001437.2:c.-91+243_-91+250del NP_001428.1:n.-91+243_-91+250del
NR_073496.1:n.654-10715_654-10708del
XM_011536545.1:c.-91+243_-91+250del XP_011534847.1:n.-91+243_-91+250del
XM_011536546.1:c.-91+7578_-91+7585del XP_011534848.1:n.-91+7578_-91+7585del
XM_017021079.1:c.-90-10715_-90-10708del XP_016876568.1:n.-90-10715_-90-10708del
XM_017021080.1:c.-90-10715_-90-10708del XP_016876569.1:n.-90-10715_-90-10708del
XM_017021081.1:c.-90-10715_-90-10708del XP_016876570.1:n.-90-10715_-90-10708del
XM_017021082.1:c.-90-10715_-90-10708del XP_016876571.1:n.-90-10715_-90-10708del
XM_017021083.1:c.-90-10715_-90-10708del XP_016876572.1:n.-90-10715_-90-10708del
XM_017021084.1:c.-90-10715_-90-10708del XP_016876573.1:n.-90-10715_-90-10708del
XR_001750187.1:n.485+243_485+250del
NM_001291712.2:c.-91+3743_-91+3750del NP_001278641.1:n.-91+3743_-91+3750del
NR_073496.2:n.717-10715_717-10708del
NM_001437.3:c.-91+243_-91+250del MANE Select NP_001428.1:n.-91+243_-91+250del