Canonical Allele Identifier: CA1673178564

Gene: ESR1

Linked Data

• dbSNP Id: rs2050990502

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.152102457_152102458insC , CM000668.2:g.152102457_152102458insC	GRCh38
NC_000006.11:g.152423592_152423593insC , CM000668.1:g.152423592_152423593insC	GRCh37
NC_000006.10:g.152465285_152465286insC	NCBI36
NG_008493.1:g.416962_416963insC
NG_008493.2:g.450767_450768insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000206249.8:c.*3491_*3492insC MANE Select	ENSP00000206249.3:n.*3491_*3492insC
ENST00000641399.1:n.1070+3537_1070+3538insC
ENST00000206249.7:c.*3491_*3492insC	ENSP00000206249.3:n.*3491_*3492insC
ENST00000427531.6:c.851-22809_851-22808insC	ENSP00000394721.2:n.851-22809_851-22808insC
ENST00000440973.5:c.*3491_*3492insC	ENSP00000405330.1:n.*3491_*3492insC
ENST00000443427.5:c.*3491_*3492insC	ENSP00000387500.1:n.*3491_*3492insC
NM_000125.3:c.*3491_*3492insC	NP_000116.2:n.*3491_*3492insC
NM_001122740.1:c.*3491_*3492insC	NP_001116212.1:n.*3491_*3492insC
NM_001122741.1:c.*3491_*3492insC	NP_001116213.1:n.*3491_*3492insC
NM_001122742.1:c.*3491_*3492insC	NP_001116214.1:n.*3491_*3492insC
NM_001291230.1:c.*3491_*3492insC	NP_001278159.1:n.*3491_*3492insC
NM_001291241.1:c.*3491_*3492insC	NP_001278170.1:n.*3491_*3492insC
XM_006715374.2:c.*3694_*3695insC	XP_006715437.1:n.*3694_*3695insC
XM_006715375.2:c.*3491_*3492insC	XP_006715438.1:n.*3491_*3492insC
XM_011535543.1:c.*3491_*3492insC	XP_011533845.1:n.*3491_*3492insC
XM_011535544.1:c.*3491_*3492insC	XP_011533846.1:n.*3491_*3492insC
XM_011535545.1:c.*3491_*3492insC	XP_011533847.1:n.*3491_*3492insC
XM_011535546.1:c.*3491_*3492insC	XP_011533848.1:n.*3491_*3492insC
XM_011535548.1:c.*3491_*3492insC	XP_011533850.1:n.*3491_*3492insC
XM_011535549.1:c.*3491_*3492insC	XP_011533851.1:n.*3491_*3492insC
NM_001328100.1:c.851-22809_851-22808insC	NP_001315029.1:n.851-22809_851-22808insC
XM_006715374.3:c.*3694_*3695insC	XP_006715437.1:n.*3694_*3695insC
NM_000125.4:c.*3491_*3492insC MANE Select	NP_000116.2:n.*3491_*3492insC
NM_001328100.2:c.851-22809_851-22808insC	NP_001315029.1:n.851-22809_851-22808insC
NM_001122740.2:c.*3491_*3492insC	NP_001116212.1:n.*3491_*3492insC
NM_001122741.2:c.*3491_*3492insC	NP_001116213.1:n.*3491_*3492insC
NM_001122742.2:c.*3491_*3492insC	NP_001116214.1:n.*3491_*3492insC
NM_001291230.2:c.*3491_*3492insC	NP_001278159.1:n.*3491_*3492insC
NM_001291241.2:c.*3491_*3492insC	NP_001278170.1:n.*3491_*3492insC
NM_001385568.1:c.*3491_*3492insC	NP_001372497.1:n.*3491_*3492insC
NM_001385569.1:c.*3491_*3492insC	NP_001372498.1:n.*3491_*3492insC
NM_001385570.1:c.*3694_*3695insC	NP_001372499.1:n.*3694_*3695insC
NM_001385571.1:c.*3694_*3695insC	NP_001372500.1:n.*3694_*3695insC
NM_001385572.1:c.*3694_*3695insC	NP_001372501.1:n.*3694_*3695insC