Canonical Allele Identifier: CA16283821
Gene: ESR1 HGNC NCBI

Linked Data

dbSNP Id: rs1884051

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151962144G>A , CM000668.2:g.151962144G>A GRCh38
NC_000006.11:g.152283279G>A , CM000668.1:g.152283279G>A GRCh37
NC_000006.10:g.152324972G>A NCBI36
NG_008493.1:g.276649G>A
NG_008493.2:g.310454G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000206249.8:c.1096+17636G>A MANE Select ENSP00000206249.3:p.=
ENST00000638569.1:n.42+17895G>A ENSP00000491412.1:p.=
ENST00000641399.1:n.424+17636G>A
ENST00000206249.7:c.1096+17636G>A ENSP00000206249.3:p.=
ENST00000338799.9:c.1096+17636G>A ENSP00000342630.5:p.=
ENST00000406599.5:c.453-98847G>A ENSP00000384064.1:p.=
ENST00000415488.1:n.116-49512G>A ENSP00000401995.1:p.=
ENST00000427531.6:c.577+17636G>A ENSP00000394721.2:p.=
ENST00000440973.5:c.1096+17636G>A ENSP00000405330.1:p.=
ENST00000443427.5:c.1096+17636G>A ENSP00000387500.1:p.=
ENST00000456483.3:c.*110+81373G>A ENSP00000415934.3:p.=
ENST00000482101.1:n.337+17636G>A
NM_000125.3:c.1096+17636G>A NP_000116.2:p.=
NM_001122740.1:c.1096+17636G>A NP_001116212.1:p.=
NM_001122741.1:c.1096+17636G>A NP_001116213.1:p.=
NM_001122742.1:c.1096+17636G>A NP_001116214.1:p.=
NM_001291230.1:c.1102+17636G>A NP_001278159.1:p.=
NM_001291241.1:c.1093+17636G>A NP_001278170.1:p.=
XM_006715374.2:c.1096+17636G>A XP_006715437.1:p.=
XM_006715375.2:c.577+17636G>A XP_006715438.1:p.=
XM_011535543.1:c.1096+17636G>A XP_011533845.1:p.=
XM_011535544.1:c.1096+17636G>A XP_011533846.1:p.=
XM_011535545.1:c.1096+17636G>A XP_011533847.1:p.=
XM_011535546.1:c.1096+17636G>A XP_011533848.1:p.=
XM_011535547.1:c.1096+17636G>A XP_011533849.1:p.=
XM_011535548.1:c.577+17636G>A XP_011533850.1:p.=
XM_011535549.1:c.367+17636G>A XP_011533851.1:p.=
NM_001328100.1:c.577+17636G>A NP_001315029.1:p.=
XM_006715374.3:c.1096+17636G>A XP_006715437.1:p.=
XM_006715375.3:c.577+17636G>A XP_006715438.1:p.=
XM_011535543.2:c.1096+17636G>A XP_011533845.1:p.=
XM_011535544.2:c.1096+17636G>A XP_011533846.1:p.=
XM_011535545.2:c.1096+17636G>A XP_011533847.1:p.=
XM_011535547.2:c.1096+17636G>A XP_011533849.1:p.=
XM_011535549.2:c.367+17636G>A XP_011533851.1:p.=
XM_017010376.1:c.1096+17636G>A XP_016865865.1:p.=
XM_017010377.1:c.1096+17636G>A XP_016865866.1:p.=
XM_017010378.1:c.1096+17636G>A XP_016865867.1:p.=
XM_017010379.1:c.1096+17636G>A XP_016865868.1:p.=
XM_017010380.1:c.1096+17636G>A XP_016865869.1:p.=
XM_017010381.1:c.1096+17636G>A XP_016865870.1:p.=
XM_017010382.2:c.439+17636G>A XP_016865871.1:p.=
XM_017010383.1:c.307+17636G>A XP_016865872.1:p.=
XR_001743223.2:n.1466+17636G>A
XR_002956266.1:n.1466+17636G>A
NM_000125.4:c.1096+17636G>A MANE Select NP_000116.2:p.=
NM_001328100.2:c.577+17636G>A NP_001315029.1:p.=
NM_001122740.2:c.1096+17636G>A NP_001116212.1:p.=
NM_001122741.2:c.1096+17636G>A NP_001116213.1:p.=
NM_001122742.2:c.1096+17636G>A NP_001116214.1:p.=
NM_001291230.2:c.1102+17636G>A NP_001278159.1:p.=
NM_001291241.2:c.1093+17636G>A NP_001278170.1:p.=
NM_001385568.1:c.1096+17636G>A NP_001372497.1:p.=
NM_001385569.1:c.1096+17636G>A NP_001372498.1:p.=
NM_001385570.1:c.1096+17636G>A NP_001372499.1:p.=
NM_001385571.1:c.1096+17636G>A NP_001372500.1:p.=
NM_001385572.1:c.1096+17636G>A NP_001372501.1:p.=