Canonical Allele Identifier: CA2625798237

Gene: ESRRB

Linked Data

• gnomAD v4: 14-76501342-C-CCGTCT

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.76501343_76501344insGTCTC , CM000676.2:g.76501343_76501344insGTCTC	GRCh38
NC_000014.8:g.76967686_76967687insGTCTC , CM000676.1:g.76967686_76967687insGTCTC	GRCh37
NC_000014.7:g.76037439_76037440insGTCTC	NCBI36
NG_012278.1:g.134997_134998insGTCTC
NG_012278.2:g.134997_134998insGTCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380887.7:c.*622_*623insGTCTC	ENSP00000370270.2:n.*622_*623insGTCTC
ENST00000644823.1:c.*2885_*2886insGTCTC MANE Select	ENSP00000493776.1:n.*2885_*2886insGTCTC
ENST00000380887.6:c.*622_*623insGTCTC	ENSP00000370270.2:n.*622_*623insGTCTC
ENST00000509242.5:c.*622_*623insGTCTC	ENSP00000422488.1:n.*622_*623insGTCTC
ENST00000611036.1:n.1698_1699insGTCTC
NM_004452.3:c.*622_*623insGTCTC	NP_004443.3:n.*622_*623insGTCTC
XM_011536547.1:c.*1118_*1119insGTCTC	XP_011534849.1:n.*1118_*1119insGTCTC
XM_011536548.1:c.*1118_*1119insGTCTC	XP_011534850.1:n.*1118_*1119insGTCTC
XM_011536549.1:c.*1118_*1119insGTCTC	XP_011534851.1:n.*1118_*1119insGTCTC
XM_011536550.1:c.*1118_*1119insGTCTC	XP_011534852.1:n.*1118_*1119insGTCTC
XM_011536551.1:c.*1118_*1119insGTCTC	XP_011534853.1:n.*1118_*1119insGTCTC
XM_011536552.1:c.*1118_*1119insGTCTC	XP_011534854.1:n.*1118_*1119insGTCTC
XM_011536553.1:c.*2381_*2382insGTCTC	XP_011534855.1:n.*2381_*2382insGTCTC
XM_011536554.1:c.*622_*623insGTCTC	XP_011534856.1:n.*622_*623insGTCTC
XM_011536555.1:c.*1118_*1119insGTCTC	XP_011534857.1:n.*1118_*1119insGTCTC
XR_943401.1:n.2646_2647insGTCTC
XR_944039.1:n.144+814_144+815insAGACG
XM_011536547.2:c.*1118_*1119insGTCTC	XP_011534849.1:n.*1118_*1119insGTCTC
XM_011536550.2:c.*1118_*1119insGTCTC	XP_011534852.1:n.*1118_*1119insGTCTC
XM_011536553.2:c.*2381_*2382insGTCTC	XP_011534855.1:n.*2381_*2382insGTCTC
XM_011536554.2:c.*622_*623insGTCTC	XP_011534856.1:n.*622_*623insGTCTC
XM_017021085.1:c.*1118_*1119insGTCTC	XP_016876574.1:n.*1118_*1119insGTCTC
XM_024449508.1:c.*1461_*1462insGTCTC	XP_024305276.1:n.*1461_*1462insGTCTC
XM_024449509.1:c.*622_*623insGTCTC	XP_024305277.1:n.*622_*623insGTCTC
XR_943401.2:n.2869_2870insGTCTC
NM_001379180.1:c.*2885_*2886insGTCTC MANE Select	NP_001366109.1:n.*2885_*2886insGTCTC
NM_004452.4:c.*622_*623insGTCTC	NP_004443.3:n.*622_*623insGTCTC