Canonical Allele Identifier: CA7225433

Gene: ESR2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.64260555G>A , CM000676.2:g.64260555G>A	GRCh38
NC_000014.8:g.64727273G>A , CM000676.1:g.64727273G>A	GRCh37
NC_000014.7:g.63797026G>A	NCBI36
NG_011535.1:g.82996C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001437.3:c.846C>T MANE Select	NP_001428.1:p.Ile282=
ENST00000341099.6:c.846C>T MANE Select	ENSP00000343925.4:p.Ile282=
NM_001040275.1:c.846C>T	NP_001035365.1:p.Ile282=
NM_001214902.1:c.846C>T	NP_001201831.1:p.Ile282=
NM_001271876.1:c.846C>T	NP_001258805.1:p.Ile282=
NM_001271877.1:c.846C>T	NP_001258806.1:p.Ile282=
NM_001291712.1:c.846C>T	NP_001278641.1:p.Ile282=
NM_001291712.2:c.846C>T	NP_001278641.1:p.Ile282=
NM_001291723.1:c.846C>T	NP_001278652.1:p.Ile282=
NM_001437.2:c.846C>T	NP_001428.1:p.Ile282=
NR_073496.1:n.1589C>T
NR_073496.2:n.1652C>T
NR_073497.1:n.763C>T
ENST00000267525.10:c.846C>T	ENSP00000267525.6:p.Ile282=
ENST00000341099.5:c.846C>T	ENSP00000343925.4:p.Ile282=
ENST00000344288.10:c.846C>T	ENSP00000345616.6:p.Ile282=
ENST00000353772.7:c.846C>T	ENSP00000335551.4:p.Ile282=
ENST00000358599.9:c.846C>T	ENSP00000351412.5:p.Ile282=
ENST00000553796.5:c.846C>T	ENSP00000452426.1:p.Ile282=
ENST00000554520.1:n.674C>T
ENST00000554572.5:c.846C>T	ENSP00000450699.1:p.Ile282=
ENST00000555278.5:c.846C>T	ENSP00000450488.1:p.Ile282=
ENST00000555483.5:n.530C>T
ENST00000556275.5:c.846C>T	ENSP00000452485.2:p.Ile282=
ENST00000557772.5:c.846C>T	ENSP00000451582.1:p.Ile282=
XM_011536545.1:c.846C>T	XP_011534847.1:p.Ile282=
XM_011536546.1:c.846C>T	XP_011534848.1:p.Ile282=
XM_017021079.1:c.846C>T	XP_016876568.1:p.Ile282=
XM_017021080.1:c.846C>T	XP_016876569.1:p.Ile282=
XM_017021081.1:c.846C>T	XP_016876570.1:p.Ile282=
XM_017021082.1:c.846C>T	XP_016876571.1:p.Ile282=
XM_017021083.1:c.846C>T	XP_016876572.1:p.Ile282=
XM_017021084.1:c.846C>T	XP_016876573.1:p.Ile282=
XR_001750187.1:n.1421C>T