Canonical Allele Identifier: CA2142596577

Gene: ESR2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.64293794A= , CM000676.2:g.64293794A=	GRCh38
NC_000014.8:g.64760512A= , CM000676.1:g.64760512A=	GRCh37
NC_000014.7:g.63830265A=	NCBI36
NG_011535.1:g.49757T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341099.6:c.-91+239T= MANE Select	ENSP00000343925.4:n.-91+239T=
ENST00000341099.5:c.-91+239T=	ENSP00000343925.4:n.-91+239T=
ENST00000353772.7:c.-91+239T=	ENSP00000335551.4:n.-91+239T=
ENST00000358599.9:c.-90-10719T=	ENSP00000351412.5:n.-90-10719T=
ENST00000554572.5:c.-91+3739T=	ENSP00000450699.1:n.-91+3739T=
ENST00000556275.5:c.-91+239T=	ENSP00000452485.2:n.-91+239T=
NM_001040275.1:c.-91+239T=	NP_001035365.1:n.-91+239T=
NM_001291712.1:c.-91+3739T=	NP_001278641.1:n.-91+3739T=
NM_001291723.1:c.-90-10719T=	NP_001278652.1:n.-90-10719T=
NM_001437.2:c.-91+239T=	NP_001428.1:n.-91+239T=
NR_073496.1:n.654-10719T=
XM_011536545.1:c.-91+239T=	XP_011534847.1:n.-91+239T=
XM_011536546.1:c.-91+7574T=	XP_011534848.1:n.-91+7574T=
XM_017021079.1:c.-90-10719T=	XP_016876568.1:n.-90-10719T=
XM_017021080.1:c.-90-10719T=	XP_016876569.1:n.-90-10719T=
XM_017021081.1:c.-90-10719T=	XP_016876570.1:n.-90-10719T=
XM_017021082.1:c.-90-10719T=	XP_016876571.1:n.-90-10719T=
XM_017021083.1:c.-90-10719T=	XP_016876572.1:n.-90-10719T=
XM_017021084.1:c.-90-10719T=	XP_016876573.1:n.-90-10719T=
XR_001750187.1:n.485+239T=
NM_001291712.2:c.-91+3739T=	NP_001278641.1:n.-91+3739T=
NR_073496.2:n.717-10719T=
NM_001437.3:c.-91+239T= MANE Select	NP_001428.1:n.-91+239T=