Canonical Allele Identifier: CA1095919353
Gene: ESR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.152101051_152101052insTTTTTTTTTTTTTTTTTTTTTTTTTTTT , CM000668.2:g.152101051_152101052insTTTTTTTTTTTTTTTTTTTTTTTTTTTT GRCh38
NC_000006.11:g.152422186_152422187insTTTTTTTTTTTTTTTTTTTTTTTTTTTT , CM000668.1:g.152422186_152422187insTTTTTTTTTTTTTTTTTTTTTTTTTTTT GRCh37
NC_000006.10:g.152463879_152463880insTTTTTTTTTTTTTTTTTTTTTTTTTTTT NCBI36
NG_008493.1:g.415556_415557insTTTTTTTTTTTTTTTTTTTTTTTTTTTT
NG_008493.2:g.449361_449362insTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Transcript Alleles

HGVS Amino-acid change
ENST00000206249.8:c.*2085_*2086insTTTTTTTTTTTTTTTTTTTTTTTTTTTT MANE Select ENSP00000206249.3:n.*2085_*2086insTTTTTTT...
ENST00000641399.1:n.1070+2131_1070+2132insTTTTTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000206249.7:c.*2085_*2086insTTTTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000206249.3:n.*2085_*2086insTTTTTTT...
ENST00000427531.6:c.851-24215_851-24214insTTTTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000394721.2:n.851-24215_851-24214in...
ENST00000440973.5:c.*2085_*2086insTTTTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000405330.1:n.*2085_*2086insTTTTTTT...
ENST00000443427.5:c.*2085_*2086insTTTTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000387500.1:n.*2085_*2086insTTTTTTT...
NM_000125.3:c.*2085_*2086insTTTTTTTTTTTTTTTTTTTTTTTTTTTT NP_000116.2:n.*2085_*2086insTTTTTTTTTTTTT...
NM_001122740.1:c.*2085_*2086insTTTTTTTTTTTTTTTTTTTTTTTTTTTT NP_001116212.1:n.*2085_*2086insTTTTTTTTTT...
NM_001122741.1:c.*2085_*2086insTTTTTTTTTTTTTTTTTTTTTTTTTTTT NP_001116213.1:n.*2085_*2086insTTTTTTTTTT...
NM_001122742.1:c.*2085_*2086insTTTTTTTTTTTTTTTTTTTTTTTTTTTT NP_001116214.1:n.*2085_*2086insTTTTTTTTTT...
NM_001291230.1:c.*2085_*2086insTTTTTTTTTTTTTTTTTTTTTTTTTTTT NP_001278159.1:n.*2085_*2086insTTTTTTTTTT...
NM_001291241.1:c.*2085_*2086insTTTTTTTTTTTTTTTTTTTTTTTTTTTT NP_001278170.1:n.*2085_*2086insTTTTTTTTTT...
XM_006715374.2:c.*2288_*2289insTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_006715437.1:n.*2288_*2289insTTTTTTTTTT...
XM_006715375.2:c.*2085_*2086insTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_006715438.1:n.*2085_*2086insTTTTTTTTTT...
XM_011535543.1:c.*2085_*2086insTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_011533845.1:n.*2085_*2086insTTTTTTTTTT...
XM_011535544.1:c.*2085_*2086insTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_011533846.1:n.*2085_*2086insTTTTTTTTTT...
XM_011535545.1:c.*2085_*2086insTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_011533847.1:n.*2085_*2086insTTTTTTTTTT...
XM_011535546.1:c.*2085_*2086insTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_011533848.1:n.*2085_*2086insTTTTTTTTTT...
XM_011535548.1:c.*2085_*2086insTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_011533850.1:n.*2085_*2086insTTTTTTTTTT...
XM_011535549.1:c.*2085_*2086insTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_011533851.1:n.*2085_*2086insTTTTTTTTTT...
NM_001328100.1:c.851-24215_851-24214insTTTTTTTTTTTTTTTTTTTTTTTTTTTT NP_001315029.1:n.851-24215_851-24214insTT...
XM_006715374.3:c.*2288_*2289insTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_006715437.1:n.*2288_*2289insTTTTTTTTTT...
NM_000125.4:c.*2085_*2086insTTTTTTTTTTTTTTTTTTTTTTTTTTTT MANE Select NP_000116.2:n.*2085_*2086insTTTTTTTTTTTTT...
NM_001328100.2:c.851-24215_851-24214insTTTTTTTTTTTTTTTTTTTTTTTTTTTT NP_001315029.1:n.851-24215_851-24214insTT...
NM_001122740.2:c.*2085_*2086insTTTTTTTTTTTTTTTTTTTTTTTTTTTT NP_001116212.1:n.*2085_*2086insTTTTTTTTTT...
NM_001122741.2:c.*2085_*2086insTTTTTTTTTTTTTTTTTTTTTTTTTTTT NP_001116213.1:n.*2085_*2086insTTTTTTTTTT...
NM_001122742.2:c.*2085_*2086insTTTTTTTTTTTTTTTTTTTTTTTTTTTT NP_001116214.1:n.*2085_*2086insTTTTTTTTTT...
NM_001291230.2:c.*2085_*2086insTTTTTTTTTTTTTTTTTTTTTTTTTTTT NP_001278159.1:n.*2085_*2086insTTTTTTTTTT...
NM_001291241.2:c.*2085_*2086insTTTTTTTTTTTTTTTTTTTTTTTTTTTT NP_001278170.1:n.*2085_*2086insTTTTTTTTTT...
NM_001385568.1:c.*2085_*2086insTTTTTTTTTTTTTTTTTTTTTTTTTTTT NP_001372497.1:n.*2085_*2086insTTTTTTTTTT...
NM_001385569.1:c.*2085_*2086insTTTTTTTTTTTTTTTTTTTTTTTTTTTT NP_001372498.1:n.*2085_*2086insTTTTTTTTTT...
NM_001385570.1:c.*2288_*2289insTTTTTTTTTTTTTTTTTTTTTTTTTTTT NP_001372499.1:n.*2288_*2289insTTTTTTTTTT...
NM_001385571.1:c.*2288_*2289insTTTTTTTTTTTTTTTTTTTTTTTTTTTT NP_001372500.1:n.*2288_*2289insTTTTTTTTTT...
NM_001385572.1:c.*2288_*2289insTTTTTTTTTTTTTTTTTTTTTTTTTTTT NP_001372501.1:n.*2288_*2289insTTTTTTTTTT...