Canonical Allele Identifier: CA2147935200

Gene: ESRRB

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.76439396_76439399delinsTTCA , CM000676.2:g.76439396_76439399delinsTTCA	GRCh38
NC_000014.8:g.76905739_76905742delinsTTCA , CM000676.1:g.76905739_76905742delinsTTCA	GRCh37
NC_000014.7:g.75975492_75975495delinsTTCA	NCBI36
NG_012278.1:g.73050_73053delinsTTCA
NG_012278.2:g.73050_73053delinsTTCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000380887.7:c.43_46delinsTTCA	ENSP00000370270.2:p.Phe15=
ENST00000505752.6:c.43_46delinsTTCA	ENSP00000423004.1:p.Phe15=
ENST00000512784.6:c.58_61delinsTTCA	ENSP00000424992.2:p.Phe20=
ENST00000644823.1:c.106_109delinsTTCA MANE Select	ENSP00000493776.1:p.Phe36=
ENST00000380887.6:c.43_46delinsTTCA	ENSP00000370270.2:p.Phe15=
ENST00000505752.5:c.43_46delinsTTCA	ENSP00000423004.1:p.Phe15=
ENST00000507951.5:n.151_154delinsTTCA
ENST00000509242.5:c.43_46delinsTTCA	ENSP00000422488.1:p.Phe15=
ENST00000512784.5:c.58_61delinsTTCA	ENSP00000424992.1:p.Phe20=
ENST00000556177.1:c.43_46delinsTTCA	ENSP00000451658.1:p.Phe15=
NM_004452.3:c.43_46delinsTTCA	NP_004443.3:p.Phe15=
XM_005267404.2:c.106_109delinsTTCA	XP_005267461.1:p.Phe36=
XM_011536547.1:c.106_109delinsTTCA	XP_011534849.1:p.Phe36=
XM_011536548.1:c.43_46delinsTTCA	XP_011534850.1:p.Phe15=
XM_011536549.1:c.43_46delinsTTCA	XP_011534851.1:p.Phe15=
XM_011536550.1:c.43_46delinsTTCA	XP_011534852.1:p.Phe15=
XM_011536551.1:c.43_46delinsTTCA	XP_011534853.1:p.Phe15=
XM_011536552.1:c.43_46delinsTTCA	XP_011534854.1:p.Phe15=
XM_011536553.1:c.106_109delinsTTCA	XP_011534855.1:p.Phe36=
XM_011536554.1:c.106_109delinsTTCA	XP_011534856.1:p.Phe36=
XR_943401.1:n.353_356delinsTTCA
XM_011536547.2:c.106_109delinsTTCA	XP_011534849.1:p.Phe36=
XM_011536550.2:c.43_46delinsTTCA	XP_011534852.1:p.Phe15=
XM_011536553.2:c.106_109delinsTTCA	XP_011534855.1:p.Phe36=
XM_011536554.2:c.106_109delinsTTCA	XP_011534856.1:p.Phe36=
XM_017021085.1:c.43_46delinsTTCA	XP_016876574.1:p.Phe15=
XM_024449508.1:c.106_109delinsTTCA	XP_024305276.1:p.Phe36=
XM_024449509.1:c.43_46delinsTTCA	XP_024305277.1:p.Phe15=
XR_001750189.1:n.576_579delinsTTCA
XR_943401.2:n.576_579delinsTTCA
NM_001379180.1:c.106_109delinsTTCA MANE Select	NP_001366109.1:p.Phe36=
NM_004452.4:c.43_46delinsTTCA	NP_004443.3:p.Phe15=