Canonical Allele Identifier: CA366085670

Gene: ESR1

Linked Data

• dbSNP Id: rs2152506444
• MyVariant Identifiers: chr6:g.152419908A>C (hg19) ; chr6:g.152098773A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.152098773A>C , CM000668.2:g.152098773A>C	GRCh38
NC_000006.11:g.152419908A>C , CM000668.1:g.152419908A>C	GRCh37
NC_000006.10:g.152461601A>C	NCBI36
NG_008493.1:g.413278A>C
NG_008493.2:g.447083A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000206249.8:c.1595A>C MANE Select	ENSP00000206249.3:p.Asn532Thr
ENST00000641399.1:n.923A>C
ENST00000206249.7:c.1595A>C	ENSP00000206249.3:p.Asn532Thr
ENST00000338799.9:c.1595A>C	ENSP00000342630.5:p.Asn532Thr
ENST00000406599.5:c.812A>C	ENSP00000384064.1:p.Asn271Thr
ENST00000427531.6:c.851-26493A>C	ENSP00000394721.2:n.851-26493A>C
ENST00000440973.5:c.1595A>C	ENSP00000405330.1:p.Asn532Thr
ENST00000443427.5:c.1595A>C	ENSP00000387500.1:p.Asn532Thr
ENST00000456483.3:c.*470A>C	ENSP00000415934.3:n.*470A>C
NM_000125.3:c.1595A>C	NP_000116.2:p.Asn532Thr
NM_001122740.1:c.1595A>C	NP_001116212.1:p.Asn532Thr
NM_001122741.1:c.1595A>C	NP_001116213.1:p.Asn532Thr
NM_001122742.1:c.1595A>C	NP_001116214.1:p.Asn532Thr
NM_001291230.1:c.1601A>C	NP_001278159.1:p.Asn534Thr
NM_001291241.1:c.1592A>C	NP_001278170.1:p.Asn531Thr
XM_006715374.2:c.*10A>C	XP_006715437.1:n.*10A>C
XM_006715375.2:c.1076A>C	XP_006715438.1:p.Asn359Thr
XM_011535543.1:c.1595A>C	XP_011533845.1:p.Asn532Thr
XM_011535544.1:c.1595A>C	XP_011533846.1:p.Asn532Thr
XM_011535545.1:c.1595A>C	XP_011533847.1:p.Asn532Thr
XM_011535546.1:c.1595A>C	XP_011533848.1:p.Asn532Thr
XM_011535548.1:c.1076A>C	XP_011533850.1:p.Asn359Thr
XM_011535549.1:c.866A>C	XP_011533851.1:p.Asn289Thr
NM_001328100.1:c.851-26493A>C	NP_001315029.1:n.851-26493A>C
XM_006715374.3:c.*10A>C	XP_006715437.1:n.*10A>C
XM_006715375.3:c.1076A>C	XP_006715438.1:p.Asn359Thr
XM_011535543.2:c.1595A>C	XP_011533845.1:p.Asn532Thr
XM_011535544.2:c.1595A>C	XP_011533846.1:p.Asn532Thr
XM_011535545.2:c.1595A>C	XP_011533847.1:p.Asn532Thr
XM_011535549.2:c.866A>C	XP_011533851.1:p.Asn289Thr
XM_017010376.1:c.1595A>C	XP_016865865.1:p.Asn532Thr
XM_017010377.1:c.1595A>C	XP_016865866.1:p.Asn532Thr
XM_017010378.1:c.1595A>C	XP_016865867.1:p.Asn532Thr
XM_017010379.1:c.1595A>C	XP_016865868.1:p.Asn532Thr
XM_017010380.1:c.1595A>C	XP_016865869.1:p.Asn532Thr
XM_017010381.1:c.1595A>C	XP_016865870.1:p.Asn532Thr
XM_017010382.2:c.938A>C	XP_016865871.1:p.Asn313Thr
XM_017010383.1:c.806A>C	XP_016865872.1:p.Asn269Thr
XR_001743223.2:n.1642A>C
NM_000125.4:c.1595A>C MANE Select	NP_000116.2:p.Asn532Thr
NM_001328100.2:c.851-26493A>C	NP_001315029.1:n.851-26493A>C
NM_001122740.2:c.1595A>C	NP_001116212.1:p.Asn532Thr
NM_001122741.2:c.1595A>C	NP_001116213.1:p.Asn532Thr
NM_001122742.2:c.1595A>C	NP_001116214.1:p.Asn532Thr
NM_001291230.2:c.1601A>C	NP_001278159.1:p.Asn534Thr
NM_001291241.2:c.1592A>C	NP_001278170.1:p.Asn531Thr
NM_001385568.1:c.1595A>C	NP_001372497.1:p.Asn532Thr
NM_001385569.1:c.1595A>C	NP_001372498.1:p.Asn532Thr
NM_001385570.1:c.*10A>C	NP_001372499.1:n.*10A>C
NM_001385571.1:c.*10A>C	NP_001372500.1:n.*10A>C
NM_001385572.1:c.*10A>C	NP_001372501.1:n.*10A>C