Canonical Allele Identifier: CA2147958511

Gene: ESRRB

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.76498317G= , CM000676.2:g.76498317G=	GRCh38
NC_000014.8:g.76964660G= , CM000676.1:g.76964660G=	GRCh37
NC_000014.7:g.76034413G=	NCBI36
NG_012278.1:g.131971G=
NG_012278.2:g.131971G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001379180.1:c.1224G= MANE Select	NP_001366109.1:p.Trp408=
ENST00000644823.1:c.1224G= MANE Select	ENSP00000493776.1:p.Trp408=
NM_004452.3:c.1161G=	NP_004443.3:p.Trp387=
NM_004452.4:c.1161G=	NP_004443.3:p.Trp387=
ENST00000380887.6:c.1161G=	ENSP00000370270.2:p.Trp387=
ENST00000380887.7:c.1161G=	ENSP00000370270.2:p.Trp387=
ENST00000505752.5:c.1161G=	ENSP00000423004.1:p.Trp387=
ENST00000505752.6:c.1161G=	ENSP00000423004.1:p.Trp387=
ENST00000509242.5:c.1161G=	ENSP00000422488.1:p.Trp387=
ENST00000512784.5:c.1176G=	ENSP00000424992.1:p.Trp392=
ENST00000512784.6:c.1176G=	ENSP00000424992.2:p.Trp392=
ENST00000556177.1:c.1161G=	ENSP00000451658.1:p.Trp387=
XM_005267404.2:c.1224G=	XP_005267461.1:p.Trp408=
XM_011536547.1:c.1224G=	XP_011534849.1:p.Trp408=
XM_011536547.2:c.1224G=	XP_011534849.1:p.Trp408=
XM_011536548.1:c.1161G=	XP_011534850.1:p.Trp387=
XM_011536549.1:c.1161G=	XP_011534851.1:p.Trp387=
XM_011536550.1:c.1161G=	XP_011534852.1:p.Trp387=
XM_011536550.2:c.1161G=	XP_011534852.1:p.Trp387=
XM_011536551.1:c.1161G=	XP_011534853.1:p.Trp387=
XM_011536552.1:c.1161G=	XP_011534854.1:p.Trp387=
XM_011536553.1:c.1224G=	XP_011534855.1:p.Trp408=
XM_011536553.2:c.1224G=	XP_011534855.1:p.Trp408=
XM_011536554.1:c.1224G=	XP_011534856.1:p.Trp408=
XM_011536554.2:c.1224G=	XP_011534856.1:p.Trp408=
XM_011536555.1:c.483G=	XP_011534857.1:p.Trp161=
XM_017021085.1:c.1161G=	XP_016876574.1:p.Trp387=
XM_024449508.1:c.1224G=	XP_024305276.1:p.Trp408=
XM_024449509.1:c.1161G=	XP_024305277.1:p.Trp387=
XR_001750189.1:n.1694G=
XR_943401.1:n.1471G=
XR_943401.2:n.1694G=
XR_944039.1:n.144+3840C=