Canonical Allele Identifier: CA919436606
Gene: ESR2 HGNC NCBI

Linked Data

dbSNP Id: rs3223460
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.64253595_64253621del , CM000676.2:g.64253595_64253621del GRCh38
NC_000014.8:g.64720313_64720339del , CM000676.1:g.64720313_64720339del GRCh37
NC_000014.7:g.63790066_63790092del NCBI36
NG_011535.1:g.89930_89956del

Transcript Alleles

HGVS Amino-acid change
ENST00000341099.6:c.1091+3605_1091+3631del MANE Select ENSP00000343925.4:n.1091+3605_1091+3631de...
ENST00000267525.10:c.952+6828_952+6854del ENSP00000267525.6:n.952+6828_952+6854del
ENST00000341099.5:c.1091+3605_1091+3631del ENSP00000343925.4:n.1091+3605_1091+3631de...
ENST00000344288.10:c.953-3942_953-3916del ENSP00000345616.6:n.953-3942_953-3916del
ENST00000353772.7:c.1091+3605_1091+3631del ENSP00000335551.4:n.1091+3605_1091+3631de...
ENST00000358599.9:c.1091+3605_1091+3631del ENSP00000351412.5:n.1091+3605_1091+3631de...
ENST00000553796.5:c.1091+3605_1091+3631del ENSP00000452426.1:n.1091+3605_1091+3631de...
ENST00000554520.1:n.780+6828_780+6854del
ENST00000554572.5:c.1091+3605_1091+3631del ENSP00000450699.1:n.1091+3605_1091+3631de...
ENST00000555278.5:c.1091+3605_1091+3631del ENSP00000450488.1:n.1091+3605_1091+3631de...
ENST00000555483.5:n.826+3605_826+3631del
ENST00000555783.1:n.218+3605_218+3631del
ENST00000556275.5:c.1091+3605_1091+3631del ENSP00000452485.2:n.1091+3605_1091+3631de...
ENST00000557772.5:c.1091+3605_1091+3631del ENSP00000451582.1:n.1091+3605_1091+3631de...
NM_001040275.1:c.1091+3605_1091+3631del NP_001035365.1:n.1091+3605_1091+3631del
NM_001214902.1:c.1091+3605_1091+3631del NP_001201831.1:n.1091+3605_1091+3631del
NM_001271876.1:c.1091+3605_1091+3631del NP_001258805.1:n.1091+3605_1091+3631del
NM_001271877.1:c.952+6828_952+6854del NP_001258806.1:n.952+6828_952+6854del
NM_001291712.1:c.1091+3605_1091+3631del NP_001278641.1:n.1091+3605_1091+3631del
NM_001291723.1:c.1091+3605_1091+3631del NP_001278652.1:n.1091+3605_1091+3631del
NM_001437.2:c.1091+3605_1091+3631del NP_001428.1:n.1091+3605_1091+3631del
NR_073496.1:n.1696-3942_1696-3916del
NR_073497.1:n.1059+3605_1059+3631del
XM_011536545.1:c.1091+3605_1091+3631del XP_011534847.1:n.1091+3605_1091+3631del
XM_011536546.1:c.1091+3605_1091+3631del XP_011534848.1:n.1091+3605_1091+3631del
XM_017021079.1:c.1091+3605_1091+3631del XP_016876568.1:n.1091+3605_1091+3631del
XM_017021080.1:c.1091+3605_1091+3631del XP_016876569.1:n.1091+3605_1091+3631del
XM_017021081.1:c.1091+3605_1091+3631del XP_016876570.1:n.1091+3605_1091+3631del
XM_017021082.1:c.1091+3605_1091+3631del XP_016876571.1:n.1091+3605_1091+3631del
XM_017021083.1:c.1091+3605_1091+3631del XP_016876572.1:n.1091+3605_1091+3631del
XM_017021084.1:c.1091+3605_1091+3631del XP_016876573.1:n.1091+3605_1091+3631del
XR_001750187.1:n.1528-3942_1528-3916del
NM_001291712.2:c.1091+3605_1091+3631del NP_001278641.1:n.1091+3605_1091+3631del
NR_073496.2:n.1759-3942_1759-3916del
NM_001437.3:c.1091+3605_1091+3631del MANE Select NP_001428.1:n.1091+3605_1091+3631del
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