Canonical Allele Identifier: CA366084321

Gene: ESR1

Linked Data

• dbSNP Id: rs2152496052
• MyVariant Identifiers: chr6:g.152415583T>A (hg19) ; chr6:g.152094448T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.152094448T>A , CM000668.2:g.152094448T>A	GRCh38
NC_000006.11:g.152415583T>A , CM000668.1:g.152415583T>A	GRCh37
NC_000006.10:g.152457276T>A	NCBI36
NG_008493.1:g.408953T>A
NG_008493.2:g.442758T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000206249.8:c.1433T>A MANE Select	ENSP00000206249.3:p.Val478Asp
ENST00000638569.1:c.43-31T>A	ENSP00000491412.1:n.43-31T>A
ENST00000641399.1:n.761T>A
ENST00000206249.7:c.1433T>A	ENSP00000206249.3:p.Val478Asp
ENST00000338799.9:c.1433T>A	ENSP00000342630.5:p.Val478Asp
ENST00000406599.5:c.650T>A	ENSP00000384064.1:p.Val217Asp
ENST00000427531.6:c.851-30818T>A	ENSP00000394721.2:n.851-30818T>A
ENST00000440973.5:c.1433T>A	ENSP00000405330.1:p.Val478Asp
ENST00000443427.5:c.1433T>A	ENSP00000387500.1:p.Val478Asp
ENST00000456483.3:c.*308T>A	ENSP00000415934.3:n.*308T>A
NM_000125.3:c.1433T>A	NP_000116.2:p.Val478Asp
NM_001122740.1:c.1433T>A	NP_001116212.1:p.Val478Asp
NM_001122741.1:c.1433T>A	NP_001116213.1:p.Val478Asp
NM_001122742.1:c.1433T>A	NP_001116214.1:p.Val478Asp
NM_001291230.1:c.1439T>A	NP_001278159.1:p.Val480Asp
NM_001291241.1:c.1430T>A	NP_001278170.1:p.Val477Asp
XM_006715374.2:c.1370-4284T>A	XP_006715437.1:n.1370-4284T>A
XM_006715375.2:c.914T>A	XP_006715438.1:p.Val305Asp
XM_011535543.1:c.1433T>A	XP_011533845.1:p.Val478Asp
XM_011535544.1:c.1433T>A	XP_011533846.1:p.Val478Asp
XM_011535545.1:c.1433T>A	XP_011533847.1:p.Val478Asp
XM_011535546.1:c.1433T>A	XP_011533848.1:p.Val478Asp
XM_011535548.1:c.914T>A	XP_011533850.1:p.Val305Asp
XM_011535549.1:c.704T>A	XP_011533851.1:p.Val235Asp
NM_001328100.1:c.851-30818T>A	NP_001315029.1:n.851-30818T>A
XM_006715374.3:c.1370-4284T>A	XP_006715437.1:n.1370-4284T>A
XM_006715375.3:c.914T>A	XP_006715438.1:p.Val305Asp
XM_011535543.2:c.1433T>A	XP_011533845.1:p.Val478Asp
XM_011535544.2:c.1433T>A	XP_011533846.1:p.Val478Asp
XM_011535545.2:c.1433T>A	XP_011533847.1:p.Val478Asp
XM_011535549.2:c.704T>A	XP_011533851.1:p.Val235Asp
XM_017010376.1:c.1433T>A	XP_016865865.1:p.Val478Asp
XM_017010377.1:c.1433T>A	XP_016865866.1:p.Val478Asp
XM_017010378.1:c.1433T>A	XP_016865867.1:p.Val478Asp
XM_017010379.1:c.1433T>A	XP_016865868.1:p.Val478Asp
XM_017010380.1:c.1433T>A	XP_016865869.1:p.Val478Asp
XM_017010381.1:c.1433T>A	XP_016865870.1:p.Val478Asp
XM_017010382.2:c.776T>A	XP_016865871.1:p.Val259Asp
XM_017010383.1:c.644T>A	XP_016865872.1:p.Val215Asp
XR_001743223.2:n.1601-4284T>A
XR_002956266.1:n.1664T>A
NM_000125.4:c.1433T>A MANE Select	NP_000116.2:p.Val478Asp
NM_001328100.2:c.851-30818T>A	NP_001315029.1:n.851-30818T>A
NM_001122740.2:c.1433T>A	NP_001116212.1:p.Val478Asp
NM_001122741.2:c.1433T>A	NP_001116213.1:p.Val478Asp
NM_001122742.2:c.1433T>A	NP_001116214.1:p.Val478Asp
NM_001291230.2:c.1439T>A	NP_001278159.1:p.Val480Asp
NM_001291241.2:c.1430T>A	NP_001278170.1:p.Val477Asp
NM_001385568.1:c.1433T>A	NP_001372497.1:p.Val478Asp
NM_001385569.1:c.1433T>A	NP_001372498.1:p.Val478Asp
NM_001385570.1:c.1370-4284T>A	NP_001372499.1:n.1370-4284T>A
NM_001385571.1:c.1370-4284T>A	NP_001372500.1:n.1370-4284T>A
NM_001385572.1:c.1370-4284T>A	NP_001372501.1:n.1370-4284T>A