Canonical Allele Identifier: CA16283828
Gene: ESR1 HGNC NCBI

Linked Data

dbSNP Id: rs3020328

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151984370C>T , CM000668.2:g.151984370C>T GRCh38
NC_000006.11:g.152305505C>T , CM000668.1:g.152305505C>T GRCh37
NC_000006.10:g.152347198C>T NCBI36
NG_008493.1:g.298875C>T
NG_008493.2:g.332680C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000206249.8:c.1097-27286C>T MANE Select ENSP00000206249.3:p.=
ENST00000638569.1:n.42+40121C>T ENSP00000491412.1:p.=
ENST00000641399.1:n.425-27286C>T
ENST00000206249.7:c.1097-27286C>T ENSP00000206249.3:p.=
ENST00000338799.9:c.1097-27286C>T ENSP00000342630.5:p.=
ENST00000406599.5:c.453-76621C>T ENSP00000384064.1:p.=
ENST00000415488.1:n.116-27286C>T ENSP00000401995.1:p.=
ENST00000427531.6:c.578-27286C>T ENSP00000394721.2:p.=
ENST00000440973.5:c.1097-27286C>T ENSP00000405330.1:p.=
ENST00000443427.5:c.1097-27286C>T ENSP00000387500.1:p.=
ENST00000456483.3:c.*111-76621C>T ENSP00000415934.3:p.=
NM_000125.3:c.1097-27286C>T NP_000116.2:p.=
NM_001122740.1:c.1097-27286C>T NP_001116212.1:p.=
NM_001122741.1:c.1097-27286C>T NP_001116213.1:p.=
NM_001122742.1:c.1097-27286C>T NP_001116214.1:p.=
NM_001291230.1:c.1103-27286C>T NP_001278159.1:p.=
NM_001291241.1:c.1094-27286C>T NP_001278170.1:p.=
XM_006715374.2:c.1097-27286C>T XP_006715437.1:p.=
XM_006715375.2:c.578-27286C>T XP_006715438.1:p.=
XM_011535543.1:c.1097-27286C>T XP_011533845.1:p.=
XM_011535544.1:c.1097-27286C>T XP_011533846.1:p.=
XM_011535545.1:c.1097-27286C>T XP_011533847.1:p.=
XM_011535546.1:c.1097-27286C>T XP_011533848.1:p.=
XM_011535547.1:c.1097-27286C>T XP_011533849.1:p.=
XM_011535548.1:c.578-27286C>T XP_011533850.1:p.=
XM_011535549.1:c.368-27286C>T XP_011533851.1:p.=
NM_001328100.1:c.578-27286C>T NP_001315029.1:p.=
XM_006715374.3:c.1097-27286C>T XP_006715437.1:p.=
XM_006715375.3:c.578-27286C>T XP_006715438.1:p.=
XM_011535543.2:c.1097-27286C>T XP_011533845.1:p.=
XM_011535544.2:c.1097-27286C>T XP_011533846.1:p.=
XM_011535545.2:c.1097-27286C>T XP_011533847.1:p.=
XM_011535547.2:c.1097-27286C>T XP_011533849.1:p.=
XM_011535549.2:c.368-27286C>T XP_011533851.1:p.=
XM_017010376.1:c.1097-27286C>T XP_016865865.1:p.=
XM_017010377.1:c.1097-27286C>T XP_016865866.1:p.=
XM_017010378.1:c.1097-27286C>T XP_016865867.1:p.=
XM_017010379.1:c.1097-27286C>T XP_016865868.1:p.=
XM_017010380.1:c.1097-27286C>T XP_016865869.1:p.=
XM_017010381.1:c.1097-27286C>T XP_016865870.1:p.=
XM_017010382.2:c.440-27286C>T XP_016865871.1:p.=
XM_017010383.1:c.308-27286C>T XP_016865872.1:p.=
XR_001743223.2:n.1466+39862C>T
XR_002956266.1:n.1466+39862C>T
NM_000125.4:c.1097-27286C>T MANE Select NP_000116.2:p.=
NM_001328100.2:c.578-27286C>T NP_001315029.1:p.=
NM_001122740.2:c.1097-27286C>T NP_001116212.1:p.=
NM_001122741.2:c.1097-27286C>T NP_001116213.1:p.=
NM_001122742.2:c.1097-27286C>T NP_001116214.1:p.=
NM_001291230.2:c.1103-27286C>T NP_001278159.1:p.=
NM_001291241.2:c.1094-27286C>T NP_001278170.1:p.=
NM_001385568.1:c.1097-27286C>T NP_001372497.1:p.=
NM_001385569.1:c.1097-27286C>T NP_001372498.1:p.=
NM_001385570.1:c.1097-27286C>T NP_001372499.1:p.=
NM_001385571.1:c.1097-27286C>T NP_001372500.1:p.=
NM_001385572.1:c.1097-27286C>T NP_001372501.1:p.=