Canonical Allele Identifier: CA1673013230

Gene: ESR1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151726844C= , CM000668.2:g.151726844C=	GRCh38
NC_000006.11:g.152047979C= , CM000668.1:g.152047979C=	GRCh37
NC_000006.10:g.152089672C=	NCBI36
NG_008493.1:g.41349C=
NG_008493.2:g.75154C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000404742.5:c.-71+24839C=	ENSP00000385373.1:n.-71+24839C=
ENST00000440973.5:c.-71+24839C=	ENSP00000405330.1:n.-71+24839C=
ENST00000473497.5:n.204+24839C=
NM_001122742.1:c.-71+24839C=	NP_001116214.1:n.-71+24839C=
XM_006715374.2:c.-71+24839C=	XP_006715437.1:n.-71+24839C=
XM_011535543.1:c.-185+24839C=	XP_011533845.1:n.-185+24839C=
XM_011535547.1:c.-71+24839C=	XP_011533849.1:n.-71+24839C=
XM_006715374.3:c.-71+24839C=	XP_006715437.1:n.-71+24839C=
XM_011535543.2:c.-185+24839C=	XP_011533845.1:n.-185+24839C=
XM_011535547.2:c.-71+24839C=	XP_011533849.1:n.-71+24839C=
XM_017010376.1:c.-71+24839C=	XP_016865865.1:n.-71+24839C=
XM_017010377.1:c.-71+24839C=	XP_016865866.1:n.-71+24839C=
XM_017010378.1:c.-71+24839C=	XP_016865867.1:n.-71+24839C=
XM_017010379.1:c.-71+24839C=	XP_016865868.1:n.-71+24839C=
XM_017010380.1:c.-71+70081C=	XP_016865869.1:n.-71+70081C=
XR_001743223.2:n.300+24839C=
XR_002956266.1:n.300+24839C=
NM_001122742.2:c.-71+24839C=	NP_001116214.1:n.-71+24839C=
NM_001385568.1:c.-71+24839C=	NP_001372497.1:n.-71+24839C=
NM_001385570.1:c.-71+24839C=	NP_001372499.1:n.-71+24839C=