Canonical Allele Identifier: CA10592754

Gene: BRCA1

Linked Data

• ClinVar Variation Id: 944868
• ClinVar RCV Id: RCV001215363 ; RCV001800970 ; RCV003316833
• dbSNP Id: rs2052738000
• MyVariant Identifiers: chr17:g.41228598G>C (hg19) ; chr17:g.43076581G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43076581G>C , CM000679.2:g.43076581G>C	GRCh38
NC_000017.10:g.41228598G>C , CM000679.1:g.41228598G>C	GRCh37
NC_000017.9:g.38482124G>C	NCBI36
NG_005905.2:g.141403C>G , LRG_292:g.141403C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000461574.2:c.4388C>G	ENSP00000417241.2:p.Pro1463Arg
ENST00000470026.6:c.4391C>G	ENSP00000419274.2:p.Pro1464Arg
ENST00000473961.6:c.4265C>G	ENSP00000420201.2:p.Pro1422Arg
ENST00000476777.6:c.4385C>G	ENSP00000417554.2:p.Pro1462Arg
ENST00000477152.6:c.4313C>G	ENSP00000419988.2:p.Pro1438Arg
ENST00000478531.6:c.1079C>G	ENSP00000420412.2:p.Pro360Arg
ENST00000489037.2:c.4313C>G	ENSP00000420781.2:p.Pro1438Arg
ENST00000493919.6:c.941C>G	ENSP00000418819.2:p.Pro314Arg
ENST00000494123.6:c.4391C>G	ENSP00000419103.2:p.Pro1464Arg
ENST00000497488.2:c.3503C>G	ENSP00000418986.2:p.Pro1168Arg
ENST00000618469.2:c.4391C>G	ENSP00000478114.2:p.Pro1464Arg
ENST00000634433.2:c.4268C>G	ENSP00000489431.2:p.Pro1423Arg
ENST00000644379.2:c.4457C>G	ENSP00000496570.2:p.Pro1486Arg
ENST00000644555.2:c.941C>G	ENSP00000494614.2:p.Pro314Arg
ENST00000652672.2:c.4250C>G	ENSP00000498906.2:p.Pro1417Arg
ENST00000484087.6:c.953C>G	ENSP00000419481.2:p.Pro318Arg
ENST00000700182.1:c.998C>G	ENSP00000514849.1:p.Pro333Arg
ENST00000357654.9:c.4391C>G MANE Select	ENSP00000350283.3:p.Pro1464Arg
ENST00000471181.7:c.4454C>G	ENSP00000418960.2:p.Pro1485Arg
ENST00000644379.1:c.778C>G
ENST00000352993.7:c.965C>G	ENSP00000312236.5:p.Pro322Arg
ENST00000357654.7:c.4391C>G	ENSP00000350283.3:p.Pro1464Arg
ENST00000461221.5:c.*4174C>G	ENSP00000418548.1:n.*4174C>G
ENST00000461574.1:c.682C>G
ENST00000468300.5:c.1079C>G	ENSP00000417148.1:p.Pro360Arg
ENST00000471181.6:c.4454C>G	ENSP00000418960.2:p.Pro1485Arg
ENST00000478531.5:c.1079C>G	ENSP00000420412.1:p.Pro360Arg
ENST00000484087.5:c.704C>G	ENSP00000419481.1:p.Pro235Arg
ENST00000487825.5:c.707C>G	ENSP00000418212.1:p.Pro236Arg
ENST00000491747.6:c.1079C>G	ENSP00000420705.2:p.Pro360Arg
ENST00000493795.5:c.4250C>G	ENSP00000418775.1:p.Pro1417Arg
ENST00000493919.5:c.941C>G	ENSP00000418819.1:p.Pro314Arg
ENST00000586385.5:c.5-12630C>G	ENSP00000465818.1:n.5-12630C>G
ENST00000591534.5:c.-43-2060C>G	ENSP00000467329.1:n.-43-2060C>G
ENST00000591849.5:c.-98-26391C>G	ENSP00000465347.1:n.-98-26391C>G
ENST00000621897.1:n.282C>G
NM_007294.3:c.4391C>G , LRG_292t1:c.4391C>G	NP_009225.1:p.Pro1464Arg
NM_007297.3:c.4250C>G	NP_009228.2:p.Pro1417Arg
NM_007298.3:c.1079C>G	NP_009229.2:p.Pro360Arg
NM_007299.3:c.1079C>G	NP_009230.2:p.Pro360Arg
NM_007300.3:c.4454C>G	NP_009231.2:p.Pro1485Arg
NR_027676.1:n.4527C>G
NM_007294.4:c.4391C>G MANE Select	NP_009225.1:p.Pro1464Arg
NM_007297.4:c.4250C>G	NP_009228.2:p.Pro1417Arg
NM_007299.4:c.1079C>G	NP_009230.2:p.Pro360Arg
NM_007300.4:c.4454C>G	NP_009231.2:p.Pro1485Arg
NR_027676.2:n.4568C>G