Canonical Allele Identifier: CA2142599731
Gene: ESR2 HGNC NCBI

Linked Data

dbSNP Id: rs2076963469

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.64296864_64296865insTTT , CM000676.2:g.64296864_64296865insTTT GRCh38
NC_000014.8:g.64763582_64763583insTTT , CM000676.1:g.64763582_64763583insTTT GRCh37
NC_000014.7:g.63833335_63833336insTTT NCBI36
NG_011535.1:g.46686_46687insAAA

Transcript Alleles

HGVS Amino-acid change
ENST00000358599.9:c.-90-13790_-90-13789insAAA ENSP00000351412.5:n.-90-13790_-90-13789in...
ENST00000554572.5:c.-91+668_-91+669insAAA ENSP00000450699.1:n.-91+668_-91+669insAAA...
NM_001291712.1:c.-91+668_-91+669insAAA NP_001278641.1:n.-91+668_-91+669insAAA
NM_001291723.1:c.-90-13790_-90-13789insAAA NP_001278652.1:n.-90-13790_-90-13789insAA...
NR_073496.1:n.654-13790_654-13789insAAA
XM_011536546.1:c.-91+4503_-91+4504insAAA XP_011534848.1:n.-91+4503_-91+4504insAAA
XM_017021079.1:c.-90-13790_-90-13789insAAA XP_016876568.1:n.-90-13790_-90-13789insAA...
XM_017021080.1:c.-90-13790_-90-13789insAAA XP_016876569.1:n.-90-13790_-90-13789insAA...
XM_017021081.1:c.-90-13790_-90-13789insAAA XP_016876570.1:n.-90-13790_-90-13789insAA...
XM_017021082.1:c.-90-13790_-90-13789insAAA XP_016876571.1:n.-90-13790_-90-13789insAA...
XM_017021083.1:c.-90-13790_-90-13789insAAA XP_016876572.1:n.-90-13790_-90-13789insAA...
XM_017021084.1:c.-90-13790_-90-13789insAAA XP_016876573.1:n.-90-13790_-90-13789insAA...
NM_001291712.2:c.-91+668_-91+669insAAA NP_001278641.1:n.-91+668_-91+669insAAA
NR_073496.2:n.717-13790_717-13789insAAA