Canonical Allele Identifier: CA1673022112

Gene: ESR1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151747229G= , CM000668.2:g.151747229G=	GRCh38
NC_000006.11:g.152068364G= , CM000668.1:g.152068364G=	GRCh37
NC_000006.10:g.152110057G=	NCBI36
NG_008493.1:g.61734G=
NG_008493.2:g.95539G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001122742.1:c.-71+45224G=	NP_001116214.1:n.-71+45224G=
NM_001122742.2:c.-71+45224G=	NP_001116214.1:n.-71+45224G=
NM_001385568.1:c.-71+45224G=	NP_001372497.1:n.-71+45224G=
NM_001385570.1:c.-71+45224G=	NP_001372499.1:n.-71+45224G=
ENST00000404742.5:c.-71+45224G=	ENSP00000385373.1:n.-71+45224G=
ENST00000440973.5:c.-71+45224G=	ENSP00000405330.1:n.-71+45224G=
ENST00000473497.5:n.204+45224G=
XM_006715374.2:c.-71+45224G=	XP_006715437.1:n.-71+45224G=
XM_006715374.3:c.-71+45224G=	XP_006715437.1:n.-71+45224G=
XM_011535543.1:c.-184-10251G=	XP_011533845.1:n.-184-10251G=
XM_011535543.2:c.-184-10251G=	XP_011533845.1:n.-184-10251G=
XM_011535547.1:c.-71+45224G=	XP_011533849.1:n.-71+45224G=
XM_011535547.2:c.-71+45224G=	XP_011533849.1:n.-71+45224G=
XM_017010376.1:c.-71+45224G=	XP_016865865.1:n.-71+45224G=
XM_017010377.1:c.-71+45224G=	XP_016865866.1:n.-71+45224G=
XM_017010378.1:c.-71+45224G=	XP_016865867.1:n.-71+45224G=
XM_017010379.1:c.-71+45224G=	XP_016865868.1:n.-71+45224G=
XM_017010380.1:c.-70-60614G=	XP_016865869.1:n.-70-60614G=
XR_001743223.2:n.300+45224G=
XR_002956266.1:n.300+45224G=