Canonical Allele Identifier: CA1673101258

Gene: ESR1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151944187C= , CM000668.2:g.151944187C=	GRCh38
NC_000006.11:g.152265322C= , CM000668.1:g.152265322C=	GRCh37
NC_000006.10:g.152307015C=	NCBI36
NG_008493.1:g.258692C=
NG_008493.2:g.292497C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000206249.8:c.775C= MANE Select	ENSP00000206249.3:p.Arg259=
ENST00000641399.1:n.103C=
ENST00000206249.7:c.775C=	ENSP00000206249.3:p.Arg259=
ENST00000338799.9:c.775C=	ENSP00000342630.5:p.Arg259=
ENST00000406599.5:c.453-116804C=	ENSP00000384064.1:n.453-116804C=
ENST00000415488.1:c.115+63416C=	ENSP00000401995.1:n.115+63416C=
ENST00000427531.6:c.256C=	ENSP00000394721.2:p.Arg86=
ENST00000440973.5:c.775C=	ENSP00000405330.1:p.Arg259=
ENST00000443427.5:c.775C=	ENSP00000387500.1:p.Arg259=
ENST00000456483.3:c.*110+63416C=	ENSP00000415934.3:n.*110+63416C=
ENST00000482101.1:n.16C=
NM_000125.3:c.775C=	NP_000116.2:p.Arg259=
NM_001122740.1:c.775C=	NP_001116212.1:p.Arg259=
NM_001122741.1:c.775C=	NP_001116213.1:p.Arg259=
NM_001122742.1:c.775C=	NP_001116214.1:p.Arg259=
NM_001291230.1:c.781C=	NP_001278159.1:p.Arg261=
NM_001291241.1:c.772C=	NP_001278170.1:p.Arg258=
XM_006715374.2:c.775C=	XP_006715437.1:p.Arg259=
XM_006715375.2:c.256C=	XP_006715438.1:p.Arg86=
XM_011535543.1:c.775C=	XP_011533845.1:p.Arg259=
XM_011535544.1:c.775C=	XP_011533846.1:p.Arg259=
XM_011535545.1:c.775C=	XP_011533847.1:p.Arg259=
XM_011535546.1:c.775C=	XP_011533848.1:p.Arg259=
XM_011535547.1:c.775C=	XP_011533849.1:p.Arg259=
XM_011535548.1:c.256C=	XP_011533850.1:p.Arg86=
XM_011535549.1:c.46C=	XP_011533851.1:p.Arg16=
NM_001328100.1:c.256C=	NP_001315029.1:p.Arg86=
XM_006715374.3:c.775C=	XP_006715437.1:p.Arg259=
XM_006715375.3:c.256C=	XP_006715438.1:p.Arg86=
XM_011535543.2:c.775C=	XP_011533845.1:p.Arg259=
XM_011535544.2:c.775C=	XP_011533846.1:p.Arg259=
XM_011535545.2:c.775C=	XP_011533847.1:p.Arg259=
XM_011535547.2:c.775C=	XP_011533849.1:p.Arg259=
XM_011535549.2:c.46C=	XP_011533851.1:p.Arg16=
XM_017010376.1:c.775C=	XP_016865865.1:p.Arg259=
XM_017010377.1:c.775C=	XP_016865866.1:p.Arg259=
XM_017010378.1:c.775C=	XP_016865867.1:p.Arg259=
XM_017010379.1:c.775C=	XP_016865868.1:p.Arg259=
XM_017010380.1:c.775C=	XP_016865869.1:p.Arg259=
XM_017010381.1:c.775C=	XP_016865870.1:p.Arg259=
XM_017010382.2:c.118C=	XP_016865871.1:p.Arg40=
XM_017010383.1:c.-15C=	XP_016865872.1:n.-15C=
XR_001743223.2:n.1145C=
XR_002956266.1:n.1145C=
NM_000125.4:c.775C= MANE Select	NP_000116.2:p.Arg259=
NM_001328100.2:c.256C=	NP_001315029.1:p.Arg86=
NM_001122740.2:c.775C=	NP_001116212.1:p.Arg259=
NM_001122741.2:c.775C=	NP_001116213.1:p.Arg259=
NM_001122742.2:c.775C=	NP_001116214.1:p.Arg259=
NM_001291230.2:c.781C=	NP_001278159.1:p.Arg261=
NM_001291241.2:c.772C=	NP_001278170.1:p.Arg258=
NM_001385568.1:c.775C=	NP_001372497.1:p.Arg259=
NM_001385569.1:c.775C=	NP_001372498.1:p.Arg259=
NM_001385570.1:c.775C=	NP_001372499.1:p.Arg259=
NM_001385571.1:c.775C=	NP_001372500.1:p.Arg259=
NM_001385572.1:c.775C=	NP_001372501.1:p.Arg259=