Canonical Allele Identifier: CA10592177

Gene: BRCA1

Linked Data

• ClinVar Variation Id: 441427
• ClinVar RCV Id: RCV000509840
• dbSNP Id: rs1555581811
• MyVariant Identifiers: chr17:g.41226356T>C (hg19) ; chr17:g.43074339T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43074339T>C , CM000679.2:g.43074339T>C	GRCh38
NC_000017.10:g.41226356T>C , CM000679.1:g.41226356T>C	GRCh37
NC_000017.9:g.38479882T>C	NCBI36
NG_005905.2:g.143645A>G , LRG_292:g.143645A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461574.2:c.4664A>G	ENSP00000417241.2:p.Gln1555Arg
ENST00000470026.6:c.4667A>G	ENSP00000419274.2:p.Gln1556Arg
ENST00000473961.6:c.4541A>G	ENSP00000420201.2:p.Gln1514Arg
ENST00000476777.6:c.4661A>G	ENSP00000417554.2:p.Gln1554Arg
ENST00000477152.6:c.4589A>G	ENSP00000419988.2:p.Gln1530Arg
ENST00000478531.6:c.1355A>G	ENSP00000420412.2:p.Gln452Arg
ENST00000489037.2:c.4589A>G	ENSP00000420781.2:p.Gln1530Arg
ENST00000493919.6:c.1217A>G	ENSP00000418819.2:p.Gln406Arg
ENST00000494123.6:c.4667A>G	ENSP00000419103.2:p.Gln1556Arg
ENST00000497488.2:c.3779A>G	ENSP00000418986.2:p.Gln1260Arg
ENST00000618469.2:c.4667A>G	ENSP00000478114.2:p.Gln1556Arg
ENST00000634433.2:c.4544A>G	ENSP00000489431.2:p.Gln1515Arg
ENST00000644379.2:c.4733A>G	ENSP00000496570.2:p.Gln1578Arg
ENST00000644555.2:c.1217A>G	ENSP00000494614.2:p.Gln406Arg
ENST00000652672.2:c.4526A>G	ENSP00000498906.2:p.Gln1509Arg
ENST00000484087.6:c.1229A>G	ENSP00000419481.2:p.Gln410Arg
ENST00000700182.1:c.1274A>G	ENSP00000514849.1:p.Gln425Arg
ENST00000357654.9:c.4667A>G MANE Select	ENSP00000350283.3:p.Gln1556Arg
ENST00000471181.7:c.4730A>G	ENSP00000418960.2:p.Gln1577Arg
ENST00000644379.1:c.1054A>G
ENST00000352993.7:c.1241A>G	ENSP00000312236.5:p.Gln414Arg
ENST00000357654.7:c.4667A>G	ENSP00000350283.3:p.Gln1556Arg
ENST00000461221.5:c.*4450A>G	ENSP00000418548.1:n.*4450A>G
ENST00000468300.5:c.1355A>G	ENSP00000417148.1:p.Gln452Arg
ENST00000471181.6:c.4730A>G	ENSP00000418960.2:p.Gln1577Arg
ENST00000478531.5:c.1355A>G	ENSP00000420412.1:p.Gln452Arg
ENST00000484087.5:c.980A>G	ENSP00000419481.1:p.Gln327Arg
ENST00000491747.6:c.1355A>G	ENSP00000420705.2:p.Gln452Arg
ENST00000493795.5:c.4526A>G	ENSP00000418775.1:p.Gln1509Arg
ENST00000493919.5:c.1217A>G	ENSP00000418819.1:p.Gln406Arg
ENST00000586385.5:c.5-10388A>G	ENSP00000465818.1:n.5-10388A>G
ENST00000591534.5:c.140A>G	ENSP00000467329.1:p.Gln47Arg
ENST00000591849.5:c.-98-24149A>G	ENSP00000465347.1:n.-98-24149A>G
NM_007294.3:c.4667A>G , LRG_292t1:c.4667A>G	NP_009225.1:p.Gln1556Arg
NM_007297.3:c.4526A>G	NP_009228.2:p.Gln1509Arg
NM_007298.3:c.1355A>G	NP_009229.2:p.Gln452Arg
NM_007299.3:c.1355A>G	NP_009230.2:p.Gln452Arg
NM_007300.3:c.4730A>G	NP_009231.2:p.Gln1577Arg
NR_027676.1:n.4803A>G
NM_007294.4:c.4667A>G MANE Select	NP_009225.1:p.Gln1556Arg
NM_007297.4:c.4526A>G	NP_009228.2:p.Gln1509Arg
NM_007299.4:c.1355A>G	NP_009230.2:p.Gln452Arg
NM_007300.4:c.4730A>G	NP_009231.2:p.Gln1577Arg
NR_027676.2:n.4844A>G