Canonical Allele Identifier: CA10592766

Gene: BRCA1

Linked Data

• MyVariant Identifiers: chr17:g.41228603T>G (hg19) ; chr17:g.43076586T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43076586T>G , CM000679.2:g.43076586T>G	GRCh38
NC_000017.10:g.41228603T>G , CM000679.1:g.41228603T>G	GRCh37
NC_000017.9:g.38482129T>G	NCBI36
NG_005905.2:g.141398A>C , LRG_292:g.141398A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461574.2:c.4383A>C	ENSP00000417241.2:p.Glu1461Asp
ENST00000470026.6:c.4386A>C	ENSP00000419274.2:p.Glu1462Asp
ENST00000473961.6:c.4260A>C	ENSP00000420201.2:p.Glu1420Asp
ENST00000476777.6:c.4380A>C	ENSP00000417554.2:p.Glu1460Asp
ENST00000477152.6:c.4308A>C	ENSP00000419988.2:p.Glu1436Asp
ENST00000478531.6:c.1074A>C	ENSP00000420412.2:p.Glu358Asp
ENST00000489037.2:c.4308A>C	ENSP00000420781.2:p.Glu1436Asp
ENST00000493919.6:c.936A>C	ENSP00000418819.2:p.Glu312Asp
ENST00000494123.6:c.4386A>C	ENSP00000419103.2:p.Glu1462Asp
ENST00000497488.2:c.3498A>C	ENSP00000418986.2:p.Glu1166Asp
ENST00000618469.2:c.4386A>C	ENSP00000478114.2:p.Glu1462Asp
ENST00000634433.2:c.4263A>C	ENSP00000489431.2:p.Glu1421Asp
ENST00000644379.2:c.4452A>C	ENSP00000496570.2:p.Glu1484Asp
ENST00000644555.2:c.936A>C	ENSP00000494614.2:p.Glu312Asp
ENST00000652672.2:c.4245A>C	ENSP00000498906.2:p.Glu1415Asp
ENST00000484087.6:c.948A>C	ENSP00000419481.2:p.Glu316Asp
ENST00000700182.1:c.993A>C	ENSP00000514849.1:p.Glu331Asp
ENST00000357654.9:c.4386A>C MANE Select	ENSP00000350283.3:p.Glu1462Asp
ENST00000471181.7:c.4449A>C	ENSP00000418960.2:p.Glu1483Asp
ENST00000644379.1:c.773A>C
ENST00000352993.7:c.960A>C	ENSP00000312236.5:p.Glu320Asp
ENST00000357654.7:c.4386A>C	ENSP00000350283.3:p.Glu1462Asp
ENST00000461221.5:c.*4169A>C	ENSP00000418548.1:n.*4169A>C
ENST00000461574.1:c.677A>C
ENST00000468300.5:c.1074A>C	ENSP00000417148.1:p.Glu358Asp
ENST00000471181.6:c.4449A>C	ENSP00000418960.2:p.Glu1483Asp
ENST00000478531.5:c.1074A>C	ENSP00000420412.1:p.Glu358Asp
ENST00000484087.5:c.699A>C	ENSP00000419481.1:p.Glu233Asp
ENST00000487825.5:c.702A>C	ENSP00000418212.1:p.Glu234Asp
ENST00000491747.6:c.1074A>C	ENSP00000420705.2:p.Glu358Asp
ENST00000493795.5:c.4245A>C	ENSP00000418775.1:p.Glu1415Asp
ENST00000493919.5:c.936A>C	ENSP00000418819.1:p.Glu312Asp
ENST00000586385.5:c.5-12635A>C	ENSP00000465818.1:n.5-12635A>C
ENST00000591534.5:c.-43-2065A>C	ENSP00000467329.1:n.-43-2065A>C
ENST00000591849.5:c.-98-26396A>C	ENSP00000465347.1:n.-98-26396A>C
ENST00000621897.1:n.277A>C
NM_007294.3:c.4386A>C , LRG_292t1:c.4386A>C	NP_009225.1:p.Glu1462Asp
NM_007297.3:c.4245A>C	NP_009228.2:p.Glu1415Asp
NM_007298.3:c.1074A>C	NP_009229.2:p.Glu358Asp
NM_007299.3:c.1074A>C	NP_009230.2:p.Glu358Asp
NM_007300.3:c.4449A>C	NP_009231.2:p.Glu1483Asp
NR_027676.1:n.4522A>C
NM_007294.4:c.4386A>C MANE Select	NP_009225.1:p.Glu1462Asp
NM_007297.4:c.4245A>C	NP_009228.2:p.Glu1415Asp
NM_007299.4:c.1074A>C	NP_009230.2:p.Glu358Asp
NM_007300.4:c.4449A>C	NP_009231.2:p.Glu1483Asp
NR_027676.2:n.4563A>C