Canonical Allele Identifier: CA2147964234

Gene: ESRRB

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.76491681_76491683delinsTTG , CM000676.2:g.76491681_76491683delinsTTG	GRCh38
NC_000014.8:g.76958024_76958026delinsTTG , CM000676.1:g.76958024_76958026delinsTTG	GRCh37
NC_000014.7:g.76027777_76027779delinsTTG	NCBI36
NG_012278.1:g.125335_125337delinsTTG
NG_012278.2:g.125335_125337delinsTTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000380887.7:c.1022_1024delinsTTG	ENSP00000370270.2:p.Phe341=
ENST00000505752.6:c.1022_1024delinsTTG	ENSP00000423004.1:p.Phe341=
ENST00000512784.6:c.1037_1039delinsTTG	ENSP00000424992.2:p.Phe346=
ENST00000644823.1:c.1085_1087delinsTTG MANE Select	ENSP00000493776.1:p.Phe362=
ENST00000380887.6:c.1022_1024delinsTTG	ENSP00000370270.2:p.Phe341=
ENST00000505752.5:c.1022_1024delinsTTG	ENSP00000423004.1:p.Phe341=
ENST00000509242.5:c.1022_1024delinsTTG	ENSP00000422488.1:p.Phe341=
ENST00000512784.5:c.1037_1039delinsTTG	ENSP00000424992.1:p.Phe346=
ENST00000556177.1:c.1022_1024delinsTTG	ENSP00000451658.1:p.Phe341=
NM_004452.3:c.1022_1024delinsTTG	NP_004443.3:p.Phe341=
XM_005267404.2:c.1085_1087delinsTTG	XP_005267461.1:p.Phe362=
XM_011536547.1:c.1085_1087delinsTTG	XP_011534849.1:p.Phe362=
XM_011536548.1:c.1022_1024delinsTTG	XP_011534850.1:p.Phe341=
XM_011536549.1:c.1022_1024delinsTTG	XP_011534851.1:p.Phe341=
XM_011536550.1:c.1022_1024delinsTTG	XP_011534852.1:p.Phe341=
XM_011536551.1:c.1022_1024delinsTTG	XP_011534853.1:p.Phe341=
XM_011536552.1:c.1022_1024delinsTTG	XP_011534854.1:p.Phe341=
XM_011536553.1:c.1085_1087delinsTTG	XP_011534855.1:p.Phe362=
XM_011536554.1:c.1085_1087delinsTTG	XP_011534856.1:p.Phe362=
XM_011536555.1:c.344_346delinsTTG	XP_011534857.1:p.Phe115=
XR_943401.1:n.1332_1334delinsTTG
XR_944039.1:n.144+10474_144+10476delinsCAA
XM_011536547.2:c.1085_1087delinsTTG	XP_011534849.1:p.Phe362=
XM_011536550.2:c.1022_1024delinsTTG	XP_011534852.1:p.Phe341=
XM_011536553.2:c.1085_1087delinsTTG	XP_011534855.1:p.Phe362=
XM_011536554.2:c.1085_1087delinsTTG	XP_011534856.1:p.Phe362=
XM_017021085.1:c.1022_1024delinsTTG	XP_016876574.1:p.Phe341=
XM_024449508.1:c.1085_1087delinsTTG	XP_024305276.1:p.Phe362=
XM_024449509.1:c.1022_1024delinsTTG	XP_024305277.1:p.Phe341=
XR_001750189.1:n.1555_1557delinsTTG
XR_943401.2:n.1555_1557delinsTTG
NM_001379180.1:c.1085_1087delinsTTG MANE Select	NP_001366109.1:p.Phe362=
NM_004452.4:c.1022_1024delinsTTG	NP_004443.3:p.Phe341=