Canonical Allele Identifier: CA10592774

Gene: BRCA1

Linked Data

• ClinVar Variation Id: 531434
• ClinVar RCV Id: RCV000637794
• dbSNP Id: rs1555582692
• MyVariant Identifiers: chr17:g.41228607C>G (hg19) ; chr17:g.43076590C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43076590C>G , CM000679.2:g.43076590C>G	GRCh38
NC_000017.10:g.41228607C>G , CM000679.1:g.41228607C>G	GRCh37
NC_000017.9:g.38482133C>G	NCBI36
NG_005905.2:g.141394G>C , LRG_292:g.141394G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461574.2:c.4379G>C	ENSP00000417241.2:p.Ser1460Thr
ENST00000470026.6:c.4382G>C	ENSP00000419274.2:p.Ser1461Thr
ENST00000473961.6:c.4256G>C	ENSP00000420201.2:p.Ser1419Thr
ENST00000476777.6:c.4376G>C	ENSP00000417554.2:p.Ser1459Thr
ENST00000477152.6:c.4304G>C	ENSP00000419988.2:p.Ser1435Thr
ENST00000478531.6:c.1070G>C	ENSP00000420412.2:p.Ser357Thr
ENST00000489037.2:c.4304G>C	ENSP00000420781.2:p.Ser1435Thr
ENST00000493919.6:c.932G>C	ENSP00000418819.2:p.Ser311Thr
ENST00000494123.6:c.4382G>C	ENSP00000419103.2:p.Ser1461Thr
ENST00000497488.2:c.3494G>C	ENSP00000418986.2:p.Ser1165Thr
ENST00000618469.2:c.4382G>C	ENSP00000478114.2:p.Ser1461Thr
ENST00000634433.2:c.4259G>C	ENSP00000489431.2:p.Ser1420Thr
ENST00000644379.2:c.4448G>C	ENSP00000496570.2:p.Ser1483Thr
ENST00000644555.2:c.932G>C	ENSP00000494614.2:p.Ser311Thr
ENST00000652672.2:c.4241G>C	ENSP00000498906.2:p.Ser1414Thr
ENST00000484087.6:c.944G>C	ENSP00000419481.2:p.Ser315Thr
ENST00000700182.1:c.989G>C	ENSP00000514849.1:p.Ser330Thr
ENST00000357654.9:c.4382G>C MANE Select	ENSP00000350283.3:p.Ser1461Thr
ENST00000471181.7:c.4445G>C	ENSP00000418960.2:p.Ser1482Thr
ENST00000644379.1:c.769G>C
ENST00000352993.7:c.956G>C	ENSP00000312236.5:p.Ser319Thr
ENST00000357654.7:c.4382G>C	ENSP00000350283.3:p.Ser1461Thr
ENST00000461221.5:c.*4165G>C	ENSP00000418548.1:n.*4165G>C
ENST00000461574.1:c.673G>C
ENST00000468300.5:c.1070G>C	ENSP00000417148.1:p.Ser357Thr
ENST00000471181.6:c.4445G>C	ENSP00000418960.2:p.Ser1482Thr
ENST00000478531.5:c.1070G>C	ENSP00000420412.1:p.Ser357Thr
ENST00000484087.5:c.695G>C	ENSP00000419481.1:p.Ser232Thr
ENST00000487825.5:c.698G>C	ENSP00000418212.1:p.Ser233Thr
ENST00000491747.6:c.1070G>C	ENSP00000420705.2:p.Ser357Thr
ENST00000493795.5:c.4241G>C	ENSP00000418775.1:p.Ser1414Thr
ENST00000493919.5:c.932G>C	ENSP00000418819.1:p.Ser311Thr
ENST00000586385.5:c.5-12639G>C	ENSP00000465818.1:n.5-12639G>C
ENST00000591534.5:c.-43-2069G>C	ENSP00000467329.1:n.-43-2069G>C
ENST00000591849.5:c.-98-26400G>C	ENSP00000465347.1:n.-98-26400G>C
ENST00000621897.1:n.273G>C
NM_007294.3:c.4382G>C , LRG_292t1:c.4382G>C	NP_009225.1:p.Ser1461Thr
NM_007297.3:c.4241G>C	NP_009228.2:p.Ser1414Thr
NM_007298.3:c.1070G>C	NP_009229.2:p.Ser357Thr
NM_007299.3:c.1070G>C	NP_009230.2:p.Ser357Thr
NM_007300.3:c.4445G>C	NP_009231.2:p.Ser1482Thr
NR_027676.1:n.4518G>C
NM_007294.4:c.4382G>C MANE Select	NP_009225.1:p.Ser1461Thr
NM_007297.4:c.4241G>C	NP_009228.2:p.Ser1414Thr
NM_007299.4:c.1070G>C	NP_009230.2:p.Ser357Thr
NM_007300.4:c.4445G>C	NP_009231.2:p.Ser1482Thr
NR_027676.2:n.4559G>C