Canonical Allele Identifier: CA1673178809

Gene: ESR1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.152102736_152102737delinsAC , CM000668.2:g.152102736_152102737delinsAC	GRCh38
NC_000006.11:g.152423871_152423872delinsAC , CM000668.1:g.152423871_152423872delinsAC	GRCh37
NC_000006.10:g.152465564_152465565delinsAC	NCBI36
NG_008493.1:g.417241_417242delinsAC
NG_008493.2:g.451046_451047delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000206249.8:c.*3770_*3771delinsAC MANE Select	ENSP00000206249.3:n.*3770_*3771delinsAC
ENST00000641399.1:n.1070+3816_1070+3817delinsAC
ENST00000206249.7:c.*3770_*3771delinsAC	ENSP00000206249.3:n.*3770_*3771delinsAC
ENST00000427531.6:c.851-22530_851-22529delinsAC	ENSP00000394721.2:n.851-22530_851-22529delinsAC
ENST00000440973.5:c.*3770_*3771delinsAC	ENSP00000405330.1:n.*3770_*3771delinsAC
ENST00000443427.5:c.*3770_*3771delinsAC	ENSP00000387500.1:n.*3770_*3771delinsAC
NM_000125.3:c.*3770_*3771delinsAC	NP_000116.2:n.*3770_*3771delinsAC
NM_001122740.1:c.*3770_*3771delinsAC	NP_001116212.1:n.*3770_*3771delinsAC
NM_001122741.1:c.*3770_*3771delinsAC	NP_001116213.1:n.*3770_*3771delinsAC
NM_001122742.1:c.*3770_*3771delinsAC	NP_001116214.1:n.*3770_*3771delinsAC
NM_001291230.1:c.*3770_*3771delinsAC	NP_001278159.1:n.*3770_*3771delinsAC
NM_001291241.1:c.*3770_*3771delinsAC	NP_001278170.1:n.*3770_*3771delinsAC
XM_006715374.2:c.*3973_*3974delinsAC	XP_006715437.1:n.*3973_*3974delinsAC
XM_006715375.2:c.*3770_*3771delinsAC	XP_006715438.1:n.*3770_*3771delinsAC
XM_011535543.1:c.*3770_*3771delinsAC	XP_011533845.1:n.*3770_*3771delinsAC
XM_011535544.1:c.*3770_*3771delinsAC	XP_011533846.1:n.*3770_*3771delinsAC
XM_011535545.1:c.*3770_*3771delinsAC	XP_011533847.1:n.*3770_*3771delinsAC
XM_011535546.1:c.*3770_*3771delinsAC	XP_011533848.1:n.*3770_*3771delinsAC
XM_011535548.1:c.*3770_*3771delinsAC	XP_011533850.1:n.*3770_*3771delinsAC
XM_011535549.1:c.*3770_*3771delinsAC	XP_011533851.1:n.*3770_*3771delinsAC
NM_001328100.1:c.851-22530_851-22529delinsAC	NP_001315029.1:n.851-22530_851-22529delinsAC
XM_006715374.3:c.*3973_*3974delinsAC	XP_006715437.1:n.*3973_*3974delinsAC
NM_000125.4:c.*3770_*3771delinsAC MANE Select	NP_000116.2:n.*3770_*3771delinsAC
NM_001328100.2:c.851-22530_851-22529delinsAC	NP_001315029.1:n.851-22530_851-22529delinsAC
NM_001122740.2:c.*3770_*3771delinsAC	NP_001116212.1:n.*3770_*3771delinsAC
NM_001122741.2:c.*3770_*3771delinsAC	NP_001116213.1:n.*3770_*3771delinsAC
NM_001122742.2:c.*3770_*3771delinsAC	NP_001116214.1:n.*3770_*3771delinsAC
NM_001291230.2:c.*3770_*3771delinsAC	NP_001278159.1:n.*3770_*3771delinsAC
NM_001291241.2:c.*3770_*3771delinsAC	NP_001278170.1:n.*3770_*3771delinsAC
NM_001385568.1:c.*3770_*3771delinsAC	NP_001372497.1:n.*3770_*3771delinsAC
NM_001385569.1:c.*3770_*3771delinsAC	NP_001372498.1:n.*3770_*3771delinsAC
NM_001385570.1:c.*3973_*3974delinsAC	NP_001372499.1:n.*3973_*3974delinsAC
NM_001385571.1:c.*3973_*3974delinsAC	NP_001372500.1:n.*3973_*3974delinsAC
NM_001385572.1:c.*3973_*3974delinsAC	NP_001372501.1:n.*3973_*3974delinsAC