Canonical Allele Identifier: CA2501516087

Gene: ESR2

Linked Data

• gnomAD v4: 14-64232123-CTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.64232124_64232125del , CM000676.2:g.64232124_64232125del	GRCh38
NC_000014.8:g.64698842_64698843del , CM000676.1:g.64698842_64698843del	GRCh37
NC_000014.7:g.63768595_63768596del	NCBI36
NG_011535.1:g.111426_111427del

Transcript Alleles

HGVS	Amino-acid change
ENST00000341099.6:c.*1012_*1013del MANE Select	ENSP00000343925.4:n.*1012_*1013del
ENST00000344288.10:c.*295+2845_*295+2846del	ENSP00000345616.6:n.*295+2845_*295+2846de...
ENST00000353772.7:c.1406+2845_1406+2846del	ENSP00000335551.4:n.1406+2845_1406+2846de...
ENST00000358599.9:c.1406+2845_1406+2846del	ENSP00000351412.5:n.1406+2845_1406+2846de...
ENST00000553796.5:c.1406+2845_1406+2846del	ENSP00000452426.1:n.1406+2845_1406+2846de...
ENST00000554572.5:c.1406+2845_1406+2846del	ENSP00000450699.1:n.1406+2845_1406+2846de...
ENST00000555278.5:c.1406+2845_1406+2846del	ENSP00000450488.1:n.1406+2845_1406+2846de...
ENST00000556275.5:c.1406+2845_1406+2846del	ENSP00000452485.2:n.1406+2845_1406+2846de...
ENST00000557772.5:c.4251_4252del	ENSP00000451582.1:n.4251_4252del
NM_001040275.1:c.1406+2845_1406+2846del	NP_001035365.1:n.1406+2845_1406+2846del
NM_001214902.1:c.1406+2845_1406+2846del	NP_001201831.1:n.1406+2845_1406+2846del
NM_001271876.1:c.1406+2845_1406+2846del	NP_001258805.1:n.1406+2845_1406+2846del
NM_001291712.1:c.1406+2845_1406+2846del	NP_001278641.1:n.1406+2845_1406+2846del
NM_001291723.1:c.1406+2845_1406+2846del	NP_001278652.1:n.1406+2845_1406+2846del
NR_073496.1:n.2010+2845_2010+2846del
XM_011536545.1:c.1406+2845_1406+2846del	XP_011534847.1:n.1406+2845_1406+2846del
XM_011536546.1:c.*1012_*1013del	XP_011534848.1:n.*1012_*1013del
XM_017021079.1:c.*1012_*1013del	XP_016876568.1:n.*1012_*1013del
XM_017021080.1:c.*1012_*1013del	XP_016876569.1:n.*1012_*1013del
XM_017021081.1:c.*1012_*1013del	XP_016876570.1:n.*1012_*1013del
XM_017021082.1:c.*1012_*1013del	XP_016876571.1:n.*1012_*1013del
XM_017021083.1:c.*1012_*1013del	XP_016876572.1:n.*1012_*1013del
XM_017021084.1:c.1406+2845_1406+2846del	XP_016876573.1:n.1406+2845_1406+2846del
XR_001750187.1:n.1842+2845_1842+2846del
NM_001291712.2:c.1406+2845_1406+2846del	NP_001278641.1:n.1406+2845_1406+2846del
NR_073496.2:n.2073+2845_2073+2846del
NM_001437.3:c.*1012_*1013del MANE Select	NP_001428.1:n.*1012_*1013del