Canonical Allele Identifier: CA1673177447

Gene: ESR1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.152101061_152101065delinsTCAAG , CM000668.2:g.152101061_152101065delinsTCAAG	GRCh38
NC_000006.11:g.152422196_152422200delinsTCAAG , CM000668.1:g.152422196_152422200delinsTCAAG	GRCh37
NC_000006.10:g.152463889_152463893delinsTCAAG	NCBI36
NG_008493.1:g.415566_415570delinsTCAAG
NG_008493.2:g.449371_449375delinsTCAAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000206249.8:c.*2095_*2099delinsTCAAG MANE Select	ENSP00000206249.3:n.*2095_*2099delinsTCAA...
ENST00000641399.1:n.1070+2141_1070+2145delinsTCAAG
ENST00000206249.7:c.*2095_*2099delinsTCAAG	ENSP00000206249.3:n.*2095_*2099delinsTCAA...
ENST00000427531.6:c.851-24205_851-24201delinsTCAAG	ENSP00000394721.2:n.851-24205_851-24201de...
ENST00000440973.5:c.*2095_*2099delinsTCAAG	ENSP00000405330.1:n.*2095_*2099delinsTCAA...
ENST00000443427.5:c.*2095_*2099delinsTCAAG	ENSP00000387500.1:n.*2095_*2099delinsTCAA...
NM_000125.3:c.*2095_*2099delinsTCAAG	NP_000116.2:n.*2095_*2099delinsTCAAG
NM_001122740.1:c.*2095_*2099delinsTCAAG	NP_001116212.1:n.*2095_*2099delinsTCAAG
NM_001122741.1:c.*2095_*2099delinsTCAAG	NP_001116213.1:n.*2095_*2099delinsTCAAG
NM_001122742.1:c.*2095_*2099delinsTCAAG	NP_001116214.1:n.*2095_*2099delinsTCAAG
NM_001291230.1:c.*2095_*2099delinsTCAAG	NP_001278159.1:n.*2095_*2099delinsTCAAG
NM_001291241.1:c.*2095_*2099delinsTCAAG	NP_001278170.1:n.*2095_*2099delinsTCAAG
XM_006715374.2:c.*2298_*2302delinsTCAAG	XP_006715437.1:n.*2298_*2302delinsTCAAG
XM_006715375.2:c.*2095_*2099delinsTCAAG	XP_006715438.1:n.*2095_*2099delinsTCAAG
XM_011535543.1:c.*2095_*2099delinsTCAAG	XP_011533845.1:n.*2095_*2099delinsTCAAG
XM_011535544.1:c.*2095_*2099delinsTCAAG	XP_011533846.1:n.*2095_*2099delinsTCAAG
XM_011535545.1:c.*2095_*2099delinsTCAAG	XP_011533847.1:n.*2095_*2099delinsTCAAG
XM_011535546.1:c.*2095_*2099delinsTCAAG	XP_011533848.1:n.*2095_*2099delinsTCAAG
XM_011535548.1:c.*2095_*2099delinsTCAAG	XP_011533850.1:n.*2095_*2099delinsTCAAG
XM_011535549.1:c.*2095_*2099delinsTCAAG	XP_011533851.1:n.*2095_*2099delinsTCAAG
NM_001328100.1:c.851-24205_851-24201delinsTCAAG	NP_001315029.1:n.851-24205_851-24201delin...
XM_006715374.3:c.*2298_*2302delinsTCAAG	XP_006715437.1:n.*2298_*2302delinsTCAAG
NM_000125.4:c.*2095_*2099delinsTCAAG MANE Select	NP_000116.2:n.*2095_*2099delinsTCAAG
NM_001328100.2:c.851-24205_851-24201delinsTCAAG	NP_001315029.1:n.851-24205_851-24201delin...
NM_001122740.2:c.*2095_*2099delinsTCAAG	NP_001116212.1:n.*2095_*2099delinsTCAAG
NM_001122741.2:c.*2095_*2099delinsTCAAG	NP_001116213.1:n.*2095_*2099delinsTCAAG
NM_001122742.2:c.*2095_*2099delinsTCAAG	NP_001116214.1:n.*2095_*2099delinsTCAAG
NM_001291230.2:c.*2095_*2099delinsTCAAG	NP_001278159.1:n.*2095_*2099delinsTCAAG
NM_001291241.2:c.*2095_*2099delinsTCAAG	NP_001278170.1:n.*2095_*2099delinsTCAAG
NM_001385568.1:c.*2095_*2099delinsTCAAG	NP_001372497.1:n.*2095_*2099delinsTCAAG
NM_001385569.1:c.*2095_*2099delinsTCAAG	NP_001372498.1:n.*2095_*2099delinsTCAAG
NM_001385570.1:c.*2298_*2302delinsTCAAG	NP_001372499.1:n.*2298_*2302delinsTCAAG
NM_001385571.1:c.*2298_*2302delinsTCAAG	NP_001372500.1:n.*2298_*2302delinsTCAAG
NM_001385572.1:c.*2298_*2302delinsTCAAG	NP_001372501.1:n.*2298_*2302delinsTCAAG