Canonical Allele Identifier: CA1673177502
Gene: ESR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.152101117T= , CM000668.2:g.152101117T= GRCh38
NC_000006.11:g.152422252T= , CM000668.1:g.152422252T= GRCh37
NC_000006.10:g.152463945T= NCBI36
NG_008493.1:g.415622T=
NG_008493.2:g.449427T=

Transcript Alleles

HGVS Amino-acid change
ENST00000206249.8:c.*2151T= MANE Select ENSP00000206249.3:n.*2151T=
ENST00000641399.1:n.1070+2197T=
ENST00000206249.7:c.*2151T= ENSP00000206249.3:n.*2151T=
ENST00000427531.6:c.851-24149T= ENSP00000394721.2:n.851-24149T=
ENST00000440973.5:c.*2151T= ENSP00000405330.1:n.*2151T=
ENST00000443427.5:c.*2151T= ENSP00000387500.1:n.*2151T=
NM_000125.3:c.*2151T= NP_000116.2:n.*2151T=
NM_001122740.1:c.*2151T= NP_001116212.1:n.*2151T=
NM_001122741.1:c.*2151T= NP_001116213.1:n.*2151T=
NM_001122742.1:c.*2151T= NP_001116214.1:n.*2151T=
NM_001291230.1:c.*2151T= NP_001278159.1:n.*2151T=
NM_001291241.1:c.*2151T= NP_001278170.1:n.*2151T=
XM_006715374.2:c.*2354T= XP_006715437.1:n.*2354T=
XM_006715375.2:c.*2151T= XP_006715438.1:n.*2151T=
XM_011535543.1:c.*2151T= XP_011533845.1:n.*2151T=
XM_011535544.1:c.*2151T= XP_011533846.1:n.*2151T=
XM_011535545.1:c.*2151T= XP_011533847.1:n.*2151T=
XM_011535546.1:c.*2151T= XP_011533848.1:n.*2151T=
XM_011535548.1:c.*2151T= XP_011533850.1:n.*2151T=
XM_011535549.1:c.*2151T= XP_011533851.1:n.*2151T=
NM_001328100.1:c.851-24149T= NP_001315029.1:n.851-24149T=
XM_006715374.3:c.*2354T= XP_006715437.1:n.*2354T=
NM_000125.4:c.*2151T= MANE Select NP_000116.2:n.*2151T=
NM_001328100.2:c.851-24149T= NP_001315029.1:n.851-24149T=
NM_001122740.2:c.*2151T= NP_001116212.1:n.*2151T=
NM_001122741.2:c.*2151T= NP_001116213.1:n.*2151T=
NM_001122742.2:c.*2151T= NP_001116214.1:n.*2151T=
NM_001291230.2:c.*2151T= NP_001278159.1:n.*2151T=
NM_001291241.2:c.*2151T= NP_001278170.1:n.*2151T=
NM_001385568.1:c.*2151T= NP_001372497.1:n.*2151T=
NM_001385569.1:c.*2151T= NP_001372498.1:n.*2151T=
NM_001385570.1:c.*2354T= NP_001372499.1:n.*2354T=
NM_001385571.1:c.*2354T= NP_001372500.1:n.*2354T=
NM_001385572.1:c.*2354T= NP_001372501.1:n.*2354T=