Canonical Allele Identifier: CA2625794530

Gene: ESRRB

Linked Data

• gnomAD v4: 14-76482818-GCCTAC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.76482821_76482825del , CM000676.2:g.76482821_76482825del	GRCh38
NC_000014.8:g.76949164_76949168del , CM000676.1:g.76949164_76949168del	GRCh37
NC_000014.7:g.76018917_76018921del	NCBI36
NG_012278.1:g.116475_116479del
NG_012278.2:g.116475_116479del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380887.7:c.787+62_787+66del	ENSP00000370270.2:n.787+62_787+66del
ENST00000505752.6:c.787+62_787+66del	ENSP00000423004.1:n.787+62_787+66del
ENST00000512784.6:c.802+62_802+66del	ENSP00000424992.2:n.802+62_802+66del
ENST00000644823.1:c.850+62_850+66del MANE Select	ENSP00000493776.1:n.850+62_850+66del
ENST00000380887.6:c.787+62_787+66del	ENSP00000370270.2:n.787+62_787+66del
ENST00000505752.5:c.787+62_787+66del	ENSP00000423004.1:n.787+62_787+66del
ENST00000509242.5:c.787+62_787+66del	ENSP00000422488.1:n.787+62_787+66del
ENST00000512784.5:c.802+62_802+66del	ENSP00000424992.1:n.802+62_802+66del
ENST00000556177.1:c.787+62_787+66del	ENSP00000451658.1:n.787+62_787+66del
NM_004452.3:c.787+62_787+66del	NP_004443.3:n.787+62_787+66del
XM_005267404.2:c.850+62_850+66del	XP_005267461.1:n.850+62_850+66del
XM_011536547.1:c.850+62_850+66del	XP_011534849.1:n.850+62_850+66del
XM_011536548.1:c.787+62_787+66del	XP_011534850.1:n.787+62_787+66del
XM_011536549.1:c.787+62_787+66del	XP_011534851.1:n.787+62_787+66del
XM_011536550.1:c.787+62_787+66del	XP_011534852.1:n.787+62_787+66del
XM_011536551.1:c.787+62_787+66del	XP_011534853.1:n.787+62_787+66del
XM_011536552.1:c.787+62_787+66del	XP_011534854.1:n.787+62_787+66del
XM_011536553.1:c.850+62_850+66del	XP_011534855.1:n.850+62_850+66del
XM_011536554.1:c.850+62_850+66del	XP_011534856.1:n.850+62_850+66del
XM_011536555.1:c.109+62_109+66del	XP_011534857.1:n.109+62_109+66del
XR_943401.1:n.1097+62_1097+66del
XR_944039.1:n.145-5983_145-5979del
XM_011536547.2:c.850+62_850+66del	XP_011534849.1:n.850+62_850+66del
XM_011536550.2:c.787+62_787+66del	XP_011534852.1:n.787+62_787+66del
XM_011536553.2:c.850+62_850+66del	XP_011534855.1:n.850+62_850+66del
XM_011536554.2:c.850+62_850+66del	XP_011534856.1:n.850+62_850+66del
XM_017021085.1:c.787+62_787+66del	XP_016876574.1:n.787+62_787+66del
XM_024449508.1:c.850+62_850+66del	XP_024305276.1:n.850+62_850+66del
XM_024449509.1:c.787+62_787+66del	XP_024305277.1:n.787+62_787+66del
XR_001750189.1:n.1320+62_1320+66del
XR_943401.2:n.1320+62_1320+66del
NM_001379180.1:c.850+62_850+66del MANE Select	NP_001366109.1:n.850+62_850+66del
NM_004452.4:c.787+62_787+66del	NP_004443.3:n.787+62_787+66del