Canonical Allele Identifier: CA452987621

Gene: ESR1

Linked Data

• dbSNP Id: rs778524912
• MyVariant Identifiers: chr6:g.152265390G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151944255G>C , CM000668.2:g.151944255G>C	GRCh38
NC_000006.11:g.152265390G>C , CM000668.1:g.152265390G>C	GRCh37
NC_000006.10:g.152307083G>C	NCBI36
NG_008493.1:g.258760G>C
NG_008493.2:g.292565G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000206249.8:c.843G>C MANE Select	ENSP00000206249.3:p.Gly281=
ENST00000638569.1:c.42+6G>C	ENSP00000491412.1:n.42+6G>C
ENST00000641399.1:n.171G>C
ENST00000206249.7:c.843G>C	ENSP00000206249.3:p.Gly281=
ENST00000338799.9:c.843G>C	ENSP00000342630.5:p.Gly281=
ENST00000406599.5:c.453-116736G>C	ENSP00000384064.1:n.453-116736G>C
ENST00000415488.1:c.115+63484G>C	ENSP00000401995.1:n.115+63484G>C
ENST00000427531.6:c.324G>C	ENSP00000394721.2:p.Gly108=
ENST00000440973.5:c.843G>C	ENSP00000405330.1:p.Gly281=
ENST00000443427.5:c.843G>C	ENSP00000387500.1:p.Gly281=
ENST00000456483.3:c.*110+63484G>C	ENSP00000415934.3:n.*110+63484G>C
ENST00000482101.1:n.84G>C
NM_000125.3:c.843G>C	NP_000116.2:p.Gly281=
NM_001122740.1:c.843G>C	NP_001116212.1:p.Gly281=
NM_001122741.1:c.843G>C	NP_001116213.1:p.Gly281=
NM_001122742.1:c.843G>C	NP_001116214.1:p.Gly281=
NM_001291230.1:c.849G>C	NP_001278159.1:p.Gly283=
NM_001291241.1:c.840G>C	NP_001278170.1:p.Gly280=
XM_006715374.2:c.843G>C	XP_006715437.1:p.Gly281=
XM_006715375.2:c.324G>C	XP_006715438.1:p.Gly108=
XM_011535543.1:c.843G>C	XP_011533845.1:p.Gly281=
XM_011535544.1:c.843G>C	XP_011533846.1:p.Gly281=
XM_011535545.1:c.843G>C	XP_011533847.1:p.Gly281=
XM_011535546.1:c.843G>C	XP_011533848.1:p.Gly281=
XM_011535547.1:c.843G>C	XP_011533849.1:p.Gly281=
XM_011535548.1:c.324G>C	XP_011533850.1:p.Gly108=
XM_011535549.1:c.114G>C	XP_011533851.1:p.Gly38=
NM_001328100.1:c.324G>C	NP_001315029.1:p.Gly108=
XM_006715374.3:c.843G>C	XP_006715437.1:p.Gly281=
XM_006715375.3:c.324G>C	XP_006715438.1:p.Gly108=
XM_011535543.2:c.843G>C	XP_011533845.1:p.Gly281=
XM_011535544.2:c.843G>C	XP_011533846.1:p.Gly281=
XM_011535545.2:c.843G>C	XP_011533847.1:p.Gly281=
XM_011535547.2:c.843G>C	XP_011533849.1:p.Gly281=
XM_011535549.2:c.114G>C	XP_011533851.1:p.Gly38=
XM_017010376.1:c.843G>C	XP_016865865.1:p.Gly281=
XM_017010377.1:c.843G>C	XP_016865866.1:p.Gly281=
XM_017010378.1:c.843G>C	XP_016865867.1:p.Gly281=
XM_017010379.1:c.843G>C	XP_016865868.1:p.Gly281=
XM_017010380.1:c.843G>C	XP_016865869.1:p.Gly281=
XM_017010381.1:c.843G>C	XP_016865870.1:p.Gly281=
XM_017010382.2:c.186G>C	XP_016865871.1:p.Gly62=
XM_017010383.1:c.54G>C	XP_016865872.1:p.Gly18=
XR_001743223.2:n.1213G>C
XR_002956266.1:n.1213G>C
NM_000125.4:c.843G>C MANE Select	NP_000116.2:p.Gly281=
NM_001328100.2:c.324G>C	NP_001315029.1:p.Gly108=
NM_001122740.2:c.843G>C	NP_001116212.1:p.Gly281=
NM_001122741.2:c.843G>C	NP_001116213.1:p.Gly281=
NM_001122742.2:c.843G>C	NP_001116214.1:p.Gly281=
NM_001291230.2:c.849G>C	NP_001278159.1:p.Gly283=
NM_001291241.2:c.840G>C	NP_001278170.1:p.Gly280=
NM_001385568.1:c.843G>C	NP_001372497.1:p.Gly281=
NM_001385569.1:c.843G>C	NP_001372498.1:p.Gly281=
NM_001385570.1:c.843G>C	NP_001372499.1:p.Gly281=
NM_001385571.1:c.843G>C	NP_001372500.1:p.Gly281=
NM_001385572.1:c.843G>C	NP_001372501.1:p.Gly281=