Canonical Allele Identifier: CA1673101053

Gene: ESR1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151944008_151944011delinsTTTC , CM000668.2:g.151944008_151944011delinsTTTC	GRCh38
NC_000006.11:g.152265143_152265146delinsTTTC , CM000668.1:g.152265143_152265146delinsTTTC	GRCh37
NC_000006.10:g.152306836_152306839delinsTTTC	NCBI36
NG_008493.1:g.258513_258516delinsTTTC
NG_008493.2:g.292318_292321delinsTTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000206249.8:c.761-165_761-162delinsTTTC MANE Select	ENSP00000206249.3:n.761-165_761-162delinsTTTC
ENST00000641399.1:n.89-165_89-162delinsTTTC
ENST00000206249.7:c.761-165_761-162delinsTTTC	ENSP00000206249.3:n.761-165_761-162delinsTTTC
ENST00000338799.9:c.761-165_761-162delinsTTTC	ENSP00000342630.5:n.761-165_761-162delinsTTTC
ENST00000406599.5:c.453-116983_453-116980delinsTTTC	ENSP00000384064.1:n.453-116983_453-116980delinsTTTC
ENST00000415488.1:c.115+63237_115+63240delinsTTTC	ENSP00000401995.1:n.115+63237_115+63240delinsTTTC
ENST00000427531.6:c.242-165_242-162delinsTTTC	ENSP00000394721.2:n.242-165_242-162delinsTTTC
ENST00000440973.5:c.761-165_761-162delinsTTTC	ENSP00000405330.1:n.761-165_761-162delinsTTTC
ENST00000443427.5:c.761-165_761-162delinsTTTC	ENSP00000387500.1:n.761-165_761-162delinsTTTC
ENST00000456483.3:c.*110+63237_*110+63240delinsTTTC	ENSP00000415934.3:n.*110+63237_*110+63240delinsTTTC
NM_000125.3:c.761-165_761-162delinsTTTC	NP_000116.2:n.761-165_761-162delinsTTTC
NM_001122740.1:c.761-165_761-162delinsTTTC	NP_001116212.1:n.761-165_761-162delinsTTTC
NM_001122741.1:c.761-165_761-162delinsTTTC	NP_001116213.1:n.761-165_761-162delinsTTTC
NM_001122742.1:c.761-165_761-162delinsTTTC	NP_001116214.1:n.761-165_761-162delinsTTTC
NM_001291230.1:c.767-165_767-162delinsTTTC	NP_001278159.1:n.767-165_767-162delinsTTTC
NM_001291241.1:c.758-165_758-162delinsTTTC	NP_001278170.1:n.758-165_758-162delinsTTTC
XM_006715374.2:c.761-165_761-162delinsTTTC	XP_006715437.1:n.761-165_761-162delinsTTTC
XM_006715375.2:c.242-165_242-162delinsTTTC	XP_006715438.1:n.242-165_242-162delinsTTTC
XM_011535543.1:c.761-165_761-162delinsTTTC	XP_011533845.1:n.761-165_761-162delinsTTTC
XM_011535544.1:c.761-165_761-162delinsTTTC	XP_011533846.1:n.761-165_761-162delinsTTTC
XM_011535545.1:c.761-165_761-162delinsTTTC	XP_011533847.1:n.761-165_761-162delinsTTTC
XM_011535546.1:c.761-165_761-162delinsTTTC	XP_011533848.1:n.761-165_761-162delinsTTTC
XM_011535547.1:c.761-165_761-162delinsTTTC	XP_011533849.1:n.761-165_761-162delinsTTTC
XM_011535548.1:c.242-165_242-162delinsTTTC	XP_011533850.1:n.242-165_242-162delinsTTTC
XM_011535549.1:c.32-165_32-162delinsTTTC	XP_011533851.1:n.32-165_32-162delinsTTTC
NM_001328100.1:c.242-165_242-162delinsTTTC	NP_001315029.1:n.242-165_242-162delinsTTTC
XM_006715374.3:c.761-165_761-162delinsTTTC	XP_006715437.1:n.761-165_761-162delinsTTTC
XM_006715375.3:c.242-165_242-162delinsTTTC	XP_006715438.1:n.242-165_242-162delinsTTTC
XM_011535543.2:c.761-165_761-162delinsTTTC	XP_011533845.1:n.761-165_761-162delinsTTTC
XM_011535544.2:c.761-165_761-162delinsTTTC	XP_011533846.1:n.761-165_761-162delinsTTTC
XM_011535545.2:c.761-165_761-162delinsTTTC	XP_011533847.1:n.761-165_761-162delinsTTTC
XM_011535547.2:c.761-165_761-162delinsTTTC	XP_011533849.1:n.761-165_761-162delinsTTTC
XM_011535549.2:c.32-165_32-162delinsTTTC	XP_011533851.1:n.32-165_32-162delinsTTTC
XM_017010376.1:c.761-165_761-162delinsTTTC	XP_016865865.1:n.761-165_761-162delinsTTTC
XM_017010377.1:c.761-165_761-162delinsTTTC	XP_016865866.1:n.761-165_761-162delinsTTTC
XM_017010378.1:c.761-165_761-162delinsTTTC	XP_016865867.1:n.761-165_761-162delinsTTTC
XM_017010379.1:c.761-165_761-162delinsTTTC	XP_016865868.1:n.761-165_761-162delinsTTTC
XM_017010380.1:c.761-165_761-162delinsTTTC	XP_016865869.1:n.761-165_761-162delinsTTTC
XM_017010381.1:c.761-165_761-162delinsTTTC	XP_016865870.1:n.761-165_761-162delinsTTTC
XM_017010382.2:c.104-165_104-162delinsTTTC	XP_016865871.1:n.104-165_104-162delinsTTTC
XM_017010383.1:c.-29-165_-29-162delinsTTTC	XP_016865872.1:n.-29-165_-29-162delinsTTTC
XR_001743223.2:n.1131-165_1131-162delinsTTTC
XR_002956266.1:n.1131-165_1131-162delinsTTTC
NM_000125.4:c.761-165_761-162delinsTTTC MANE Select	NP_000116.2:n.761-165_761-162delinsTTTC
NM_001328100.2:c.242-165_242-162delinsTTTC	NP_001315029.1:n.242-165_242-162delinsTTTC
NM_001122740.2:c.761-165_761-162delinsTTTC	NP_001116212.1:n.761-165_761-162delinsTTTC
NM_001122741.2:c.761-165_761-162delinsTTTC	NP_001116213.1:n.761-165_761-162delinsTTTC
NM_001122742.2:c.761-165_761-162delinsTTTC	NP_001116214.1:n.761-165_761-162delinsTTTC
NM_001291230.2:c.767-165_767-162delinsTTTC	NP_001278159.1:n.767-165_767-162delinsTTTC
NM_001291241.2:c.758-165_758-162delinsTTTC	NP_001278170.1:n.758-165_758-162delinsTTTC
NM_001385568.1:c.761-165_761-162delinsTTTC	NP_001372497.1:n.761-165_761-162delinsTTTC
NM_001385569.1:c.761-165_761-162delinsTTTC	NP_001372498.1:n.761-165_761-162delinsTTTC
NM_001385570.1:c.761-165_761-162delinsTTTC	NP_001372499.1:n.761-165_761-162delinsTTTC
NM_001385571.1:c.761-165_761-162delinsTTTC	NP_001372500.1:n.761-165_761-162delinsTTTC
NM_001385572.1:c.761-165_761-162delinsTTTC	NP_001372501.1:n.761-165_761-162delinsTTTC