Canonical Allele Identifier: CA366213299

Gene: ESR1

Linked Data

• dbSNP Id: rs1419894030
• MyVariant Identifiers: chr6:g.152265467C>T (hg19) ; chr6:g.151944332C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151944332C>T , CM000668.2:g.151944332C>T	GRCh38
NC_000006.11:g.152265467C>T , CM000668.1:g.152265467C>T	GRCh37
NC_000006.10:g.152307160C>T	NCBI36
NG_008493.1:g.258837C>T
NG_008493.2:g.292642C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000206249.8:c.920C>T MANE Select	ENSP00000206249.3:p.Ala307Val
ENST00000638569.1:c.42+83C>T	ENSP00000491412.1:n.42+83C>T
ENST00000641399.1:n.248C>T
ENST00000206249.7:c.920C>T	ENSP00000206249.3:p.Ala307Val
ENST00000338799.9:c.920C>T	ENSP00000342630.5:p.Ala307Val
ENST00000406599.5:c.453-116659C>T	ENSP00000384064.1:n.453-116659C>T
ENST00000415488.1:c.115+63561C>T	ENSP00000401995.1:n.115+63561C>T
ENST00000427531.6:c.401C>T	ENSP00000394721.2:p.Ala134Val
ENST00000440973.5:c.920C>T	ENSP00000405330.1:p.Ala307Val
ENST00000443427.5:c.920C>T	ENSP00000387500.1:p.Ala307Val
ENST00000456483.3:c.*110+63561C>T	ENSP00000415934.3:n.*110+63561C>T
ENST00000482101.1:n.161C>T
NM_000125.3:c.920C>T	NP_000116.2:p.Ala307Val
NM_001122740.1:c.920C>T	NP_001116212.1:p.Ala307Val
NM_001122741.1:c.920C>T	NP_001116213.1:p.Ala307Val
NM_001122742.1:c.920C>T	NP_001116214.1:p.Ala307Val
NM_001291230.1:c.926C>T	NP_001278159.1:p.Ala309Val
NM_001291241.1:c.917C>T	NP_001278170.1:p.Ala306Val
XM_006715374.2:c.920C>T	XP_006715437.1:p.Ala307Val
XM_006715375.2:c.401C>T	XP_006715438.1:p.Ala134Val
XM_011535543.1:c.920C>T	XP_011533845.1:p.Ala307Val
XM_011535544.1:c.920C>T	XP_011533846.1:p.Ala307Val
XM_011535545.1:c.920C>T	XP_011533847.1:p.Ala307Val
XM_011535546.1:c.920C>T	XP_011533848.1:p.Ala307Val
XM_011535547.1:c.920C>T	XP_011533849.1:p.Ala307Val
XM_011535548.1:c.401C>T	XP_011533850.1:p.Ala134Val
XM_011535549.1:c.191C>T	XP_011533851.1:p.Ala64Val
NM_001328100.1:c.401C>T	NP_001315029.1:p.Ala134Val
XM_006715374.3:c.920C>T	XP_006715437.1:p.Ala307Val
XM_006715375.3:c.401C>T	XP_006715438.1:p.Ala134Val
XM_011535543.2:c.920C>T	XP_011533845.1:p.Ala307Val
XM_011535544.2:c.920C>T	XP_011533846.1:p.Ala307Val
XM_011535545.2:c.920C>T	XP_011533847.1:p.Ala307Val
XM_011535547.2:c.920C>T	XP_011533849.1:p.Ala307Val
XM_011535549.2:c.191C>T	XP_011533851.1:p.Ala64Val
XM_017010376.1:c.920C>T	XP_016865865.1:p.Ala307Val
XM_017010377.1:c.920C>T	XP_016865866.1:p.Ala307Val
XM_017010378.1:c.920C>T	XP_016865867.1:p.Ala307Val
XM_017010379.1:c.920C>T	XP_016865868.1:p.Ala307Val
XM_017010380.1:c.920C>T	XP_016865869.1:p.Ala307Val
XM_017010381.1:c.920C>T	XP_016865870.1:p.Ala307Val
XM_017010382.2:c.263C>T	XP_016865871.1:p.Ala88Val
XM_017010383.1:c.131C>T	XP_016865872.1:p.Ala44Val
XR_001743223.2:n.1290C>T
XR_002956266.1:n.1290C>T
NM_000125.4:c.920C>T MANE Select	NP_000116.2:p.Ala307Val
NM_001328100.2:c.401C>T	NP_001315029.1:p.Ala134Val
NM_001122740.2:c.920C>T	NP_001116212.1:p.Ala307Val
NM_001122741.2:c.920C>T	NP_001116213.1:p.Ala307Val
NM_001122742.2:c.920C>T	NP_001116214.1:p.Ala307Val
NM_001291230.2:c.926C>T	NP_001278159.1:p.Ala309Val
NM_001291241.2:c.917C>T	NP_001278170.1:p.Ala306Val
NM_001385568.1:c.920C>T	NP_001372497.1:p.Ala307Val
NM_001385569.1:c.920C>T	NP_001372498.1:p.Ala307Val
NM_001385570.1:c.920C>T	NP_001372499.1:p.Ala307Val
NM_001385571.1:c.920C>T	NP_001372500.1:p.Ala307Val
NM_001385572.1:c.920C>T	NP_001372501.1:p.Ala307Val