Canonical Allele Identifier: CA2142599765
Gene: ESR2 HGNC NCBI

Linked Data

dbSNP Id: rs2076964130

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.64296907_64296908del , CM000676.2:g.64296907_64296908del GRCh38
NC_000014.8:g.64763625_64763626del , CM000676.1:g.64763625_64763626del GRCh37
NC_000014.7:g.63833378_63833379del NCBI36
NG_011535.1:g.46644_46645del

Transcript Alleles

HGVS Amino-acid Change
ENST00000358599.9:c.-90-13832_-90-13831del ENSP00000351412.5:n.-90-13832_-90-13831del
ENST00000554572.5:c.-91+626_-91+627del ENSP00000450699.1:n.-91+626_-91+627del
NM_001291712.1:c.-91+626_-91+627del NP_001278641.1:n.-91+626_-91+627del
NM_001291723.1:c.-90-13832_-90-13831del NP_001278652.1:n.-90-13832_-90-13831del
NR_073496.1:n.654-13832_654-13831del
XM_011536546.1:c.-91+4461_-91+4462del XP_011534848.1:n.-91+4461_-91+4462del
XM_017021079.1:c.-90-13832_-90-13831del XP_016876568.1:n.-90-13832_-90-13831del
XM_017021080.1:c.-90-13832_-90-13831del XP_016876569.1:n.-90-13832_-90-13831del
XM_017021081.1:c.-90-13832_-90-13831del XP_016876570.1:n.-90-13832_-90-13831del
XM_017021082.1:c.-90-13832_-90-13831del XP_016876571.1:n.-90-13832_-90-13831del
XM_017021083.1:c.-90-13832_-90-13831del XP_016876572.1:n.-90-13832_-90-13831del
XM_017021084.1:c.-90-13832_-90-13831del XP_016876573.1:n.-90-13832_-90-13831del
NM_001291712.2:c.-91+626_-91+627del NP_001278641.1:n.-91+626_-91+627del
NR_073496.2:n.717-13832_717-13831del