Canonical Allele Identifier: CA2680805974

Gene: ESR1

Linked Data

• gnomAD v4: 6-152061194-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.152061195del , CM000668.2:g.152061195del	GRCh38
NC_000006.11:g.152382330del , CM000668.1:g.152382330del	GRCh37
NC_000006.10:g.152424023del	NCBI36
NG_008493.1:g.375700del
NG_008493.2:g.409505del

Transcript Alleles

HGVS	Amino-acid change
ENST00000206249.8:c.1369+71del MANE Select	ENSP00000206249.3:n.1369+71del
ENST00000638569.1:c.43-33284del	ENSP00000491412.1:n.43-33284del
ENST00000641399.1:n.697+71del
ENST00000206249.7:c.1369+71del	ENSP00000206249.3:n.1369+71del
ENST00000338799.9:c.1369+71del	ENSP00000342630.5:n.1369+71del
ENST00000406599.5:c.586+71del	ENSP00000384064.1:n.586+71del
ENST00000427531.6:c.850+71del	ENSP00000394721.2:n.850+71del
ENST00000440973.5:c.1369+71del	ENSP00000405330.1:n.1369+71del
ENST00000443427.5:c.1369+71del	ENSP00000387500.1:n.1369+71del
ENST00000456483.3:c.*244+71del	ENSP00000415934.3:n.*244+71del
NM_000125.3:c.1369+71del	NP_000116.2:n.1369+71del
NM_001122740.1:c.1369+71del	NP_001116212.1:n.1369+71del
NM_001122741.1:c.1369+71del	NP_001116213.1:n.1369+71del
NM_001122742.1:c.1369+71del	NP_001116214.1:n.1369+71del
NM_001291230.1:c.1375+71del	NP_001278159.1:n.1375+71del
NM_001291241.1:c.1366+71del	NP_001278170.1:n.1366+71del
XM_006715374.2:c.1369+71del	XP_006715437.1:n.1369+71del
XM_006715375.2:c.850+71del	XP_006715438.1:n.850+71del
XM_011535543.1:c.1369+71del	XP_011533845.1:n.1369+71del
XM_011535544.1:c.1369+71del	XP_011533846.1:n.1369+71del
XM_011535545.1:c.1369+71del	XP_011533847.1:n.1369+71del
XM_011535546.1:c.1369+71del	XP_011533848.1:n.1369+71del
XM_011535547.1:c.1369+71del	XP_011533849.1:n.1369+71del
XM_011535548.1:c.850+71del	XP_011533850.1:n.850+71del
XM_011535549.1:c.640+71del	XP_011533851.1:n.640+71del
XR_943116.1:n.7309del
NM_001328100.1:c.850+71del	NP_001315029.1:n.850+71del
XM_006715374.3:c.1369+71del	XP_006715437.1:n.1369+71del
XM_006715375.3:c.850+71del	XP_006715438.1:n.850+71del
XM_011535543.2:c.1369+71del	XP_011533845.1:n.1369+71del
XM_011535544.2:c.1369+71del	XP_011533846.1:n.1369+71del
XM_011535545.2:c.1369+71del	XP_011533847.1:n.1369+71del
XM_011535547.2:c.1369+71del	XP_011533849.1:n.1369+71del
XM_011535549.2:c.640+71del	XP_011533851.1:n.640+71del
XM_017010376.1:c.1369+71del	XP_016865865.1:n.1369+71del
XM_017010377.1:c.1369+71del	XP_016865866.1:n.1369+71del
XM_017010378.1:c.1369+71del	XP_016865867.1:n.1369+71del
XM_017010379.1:c.1369+71del	XP_016865868.1:n.1369+71del
XM_017010380.1:c.1369+71del	XP_016865869.1:n.1369+71del
XM_017010381.1:c.1369+71del	XP_016865870.1:n.1369+71del
XM_017010382.2:c.712+71del	XP_016865871.1:n.712+71del
XM_017010383.1:c.580+71del	XP_016865872.1:n.580+71del
XR_001743223.2:n.1600+71del
XR_002956266.1:n.1600+71del
NM_000125.4:c.1369+71del MANE Select	NP_000116.2:n.1369+71del
NM_001328100.2:c.850+71del	NP_001315029.1:n.850+71del
NM_001122740.2:c.1369+71del	NP_001116212.1:n.1369+71del
NM_001122741.2:c.1369+71del	NP_001116213.1:n.1369+71del
NM_001122742.2:c.1369+71del	NP_001116214.1:n.1369+71del
NM_001291230.2:c.1375+71del	NP_001278159.1:n.1375+71del
NM_001291241.2:c.1366+71del	NP_001278170.1:n.1366+71del
NM_001385568.1:c.1369+71del	NP_001372497.1:n.1369+71del
NM_001385569.1:c.1369+71del	NP_001372498.1:n.1369+71del
NM_001385570.1:c.1369+71del	NP_001372499.1:n.1369+71del
NM_001385571.1:c.1369+71del	NP_001372500.1:n.1369+71del
NM_001385572.1:c.1369+71del	NP_001372501.1:n.1369+71del