Canonical Allele Identifier: CA2625798360

Gene: ESRRB

Linked Data

• gnomAD v4: 14-76501390-A-AAGG

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.76501390_76501391insAGG , CM000676.2:g.76501390_76501391insAGG	GRCh38
NC_000014.8:g.76967733_76967734insAGG , CM000676.1:g.76967733_76967734insAGG	GRCh37
NC_000014.7:g.76037486_76037487insAGG	NCBI36
NG_012278.1:g.135044_135045insAGG
NG_012278.2:g.135044_135045insAGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000380887.7:c.*669_*670insAGG	ENSP00000370270.2:n.*669_*670insAGG
ENST00000644823.1:c.*2932_*2933insAGG MANE Select	ENSP00000493776.1:n.*2932_*2933insAGG
ENST00000380887.6:c.*669_*670insAGG	ENSP00000370270.2:n.*669_*670insAGG
ENST00000509242.5:c.*669_*670insAGG	ENSP00000422488.1:n.*669_*670insAGG
ENST00000611036.1:n.1745_1746insAGG
NM_004452.3:c.*669_*670insAGG	NP_004443.3:n.*669_*670insAGG
XM_011536547.1:c.*1165_*1166insAGG	XP_011534849.1:n.*1165_*1166insAGG
XM_011536548.1:c.*1165_*1166insAGG	XP_011534850.1:n.*1165_*1166insAGG
XM_011536549.1:c.*1165_*1166insAGG	XP_011534851.1:n.*1165_*1166insAGG
XM_011536550.1:c.*1165_*1166insAGG	XP_011534852.1:n.*1165_*1166insAGG
XM_011536551.1:c.*1165_*1166insAGG	XP_011534853.1:n.*1165_*1166insAGG
XM_011536552.1:c.*1165_*1166insAGG	XP_011534854.1:n.*1165_*1166insAGG
XM_011536553.1:c.*2428_*2429insAGG	XP_011534855.1:n.*2428_*2429insAGG
XM_011536554.1:c.*669_*670insAGG	XP_011534856.1:n.*669_*670insAGG
XM_011536555.1:c.*1165_*1166insAGG	XP_011534857.1:n.*1165_*1166insAGG
XR_943401.1:n.2693_2694insAGG
XR_944039.1:n.144+766_144+767insCCT
XM_011536547.2:c.*1165_*1166insAGG	XP_011534849.1:n.*1165_*1166insAGG
XM_011536550.2:c.*1165_*1166insAGG	XP_011534852.1:n.*1165_*1166insAGG
XM_011536553.2:c.*2428_*2429insAGG	XP_011534855.1:n.*2428_*2429insAGG
XM_011536554.2:c.*669_*670insAGG	XP_011534856.1:n.*669_*670insAGG
XM_017021085.1:c.*1165_*1166insAGG	XP_016876574.1:n.*1165_*1166insAGG
XM_024449508.1:c.*1508_*1509insAGG	XP_024305276.1:n.*1508_*1509insAGG
XM_024449509.1:c.*669_*670insAGG	XP_024305277.1:n.*669_*670insAGG
XR_943401.2:n.2916_2917insAGG
NM_001379180.1:c.*2932_*2933insAGG MANE Select	NP_001366109.1:n.*2932_*2933insAGG
NM_004452.4:c.*669_*670insAGG	NP_004443.3:n.*669_*670insAGG