Canonical Allele Identifier: CA2142599711

Gene: ESR2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.64296839_64296840delinsAG , CM000676.2:g.64296839_64296840delinsAG	GRCh38
NC_000014.8:g.64763557_64763558delinsAG , CM000676.1:g.64763557_64763558delinsAG	GRCh37
NC_000014.7:g.63833310_63833311delinsAG	NCBI36
NG_011535.1:g.46711_46712delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000358599.9:c.-90-13765_-90-13764delinsCT	ENSP00000351412.5:n.-90-13765_-90-13764de...
ENST00000554572.5:c.-91+693_-91+694delinsCT	ENSP00000450699.1:n.-91+693_-91+694delins...
NM_001291712.1:c.-91+693_-91+694delinsCT	NP_001278641.1:n.-91+693_-91+694delinsCT
NM_001291723.1:c.-90-13765_-90-13764delinsCT	NP_001278652.1:n.-90-13765_-90-13764delin...
NR_073496.1:n.654-13765_654-13764delinsCT
XM_011536546.1:c.-91+4528_-91+4529delinsCT	XP_011534848.1:n.-91+4528_-91+4529delinsC...
XM_017021079.1:c.-90-13765_-90-13764delinsCT	XP_016876568.1:n.-90-13765_-90-13764delin...
XM_017021080.1:c.-90-13765_-90-13764delinsCT	XP_016876569.1:n.-90-13765_-90-13764delin...
XM_017021081.1:c.-90-13765_-90-13764delinsCT	XP_016876570.1:n.-90-13765_-90-13764delin...
XM_017021082.1:c.-90-13765_-90-13764delinsCT	XP_016876571.1:n.-90-13765_-90-13764delin...
XM_017021083.1:c.-90-13765_-90-13764delinsCT	XP_016876572.1:n.-90-13765_-90-13764delin...
XM_017021084.1:c.-90-13765_-90-13764delinsCT	XP_016876573.1:n.-90-13765_-90-13764delin...
NM_001291712.2:c.-91+693_-91+694delinsCT	NP_001278641.1:n.-91+693_-91+694delinsCT
NR_073496.2:n.717-13765_717-13764delinsCT