Canonical Allele Identifier: CA10591857

Gene: BRCA1

Linked Data

• dbSNP Id: rs2153834811
• MyVariant Identifiers: chr17:g.41223099G>T (hg19) ; chr17:g.43071082G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43071082G>T , CM000679.2:g.43071082G>T	GRCh38
NC_000017.10:g.41223099G>T , CM000679.1:g.41223099G>T	GRCh37
NC_000017.9:g.38476625G>T	NCBI36
NG_005905.2:g.146902C>A , LRG_292:g.146902C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000461574.2:c.4829C>A	ENSP00000417241.2:p.Ala1610Asp
ENST00000470026.6:c.4832C>A	ENSP00000419274.2:p.Ala1611Asp
ENST00000473961.6:c.4706C>A	ENSP00000420201.2:p.Ala1569Asp
ENST00000476777.6:c.4826C>A	ENSP00000417554.2:p.Ala1609Asp
ENST00000477152.6:c.4754C>A	ENSP00000419988.2:p.Ala1585Asp
ENST00000478531.6:c.1520C>A	ENSP00000420412.2:p.Ala507Asp
ENST00000489037.2:c.4754C>A	ENSP00000420781.2:p.Ala1585Asp
ENST00000493919.6:c.1382C>A	ENSP00000418819.2:p.Ala461Asp
ENST00000494123.6:c.4832C>A	ENSP00000419103.2:p.Ala1611Asp
ENST00000497488.2:c.3944C>A	ENSP00000418986.2:p.Ala1315Asp
ENST00000618469.2:c.4832C>A	ENSP00000478114.2:p.Ala1611Asp
ENST00000634433.2:c.4709C>A	ENSP00000489431.2:p.Ala1570Asp
ENST00000644379.2:c.4898C>A	ENSP00000496570.2:p.Ala1633Asp
ENST00000644555.2:c.1382C>A	ENSP00000494614.2:p.Ala461Asp
ENST00000652672.2:c.4691C>A	ENSP00000498906.2:p.Ala1564Asp
ENST00000484087.6:c.1394C>A	ENSP00000419481.2:p.Ala465Asp
ENST00000700182.1:c.1439C>A	ENSP00000514849.1:p.Ala480Asp
ENST00000357654.9:c.4832C>A MANE Select	ENSP00000350283.3:p.Ala1611Asp
ENST00000471181.7:c.4895C>A	ENSP00000418960.2:p.Ala1632Asp
ENST00000644379.1:c.1219C>A
ENST00000352993.7:c.1406C>A	ENSP00000312236.5:p.Ala469Asp
ENST00000357654.7:c.4832C>A	ENSP00000350283.3:p.Ala1611Asp
ENST00000461221.5:c.*4615C>A	ENSP00000418548.1:n.*4615C>A
ENST00000468300.5:c.1520C>A	ENSP00000417148.1:p.Ala507Asp
ENST00000471181.6:c.4895C>A	ENSP00000418960.2:p.Ala1632Asp
ENST00000478531.5:c.1520C>A	ENSP00000420412.1:p.Ala507Asp
ENST00000484087.5:c.1145C>A	ENSP00000419481.1:p.Ala382Asp
ENST00000491747.6:c.1520C>A	ENSP00000420705.2:p.Ala507Asp
ENST00000493795.5:c.4691C>A	ENSP00000418775.1:p.Ala1564Asp
ENST00000493919.5:c.1382C>A	ENSP00000418819.1:p.Ala461Asp
ENST00000586385.5:c.5-7131C>A	ENSP00000465818.1:n.5-7131C>A
ENST00000591534.5:c.305C>A	ENSP00000467329.1:p.Ala102Asp
ENST00000591849.5:c.-98-20892C>A	ENSP00000465347.1:n.-98-20892C>A
NM_007294.3:c.4832C>A , LRG_292t1:c.4832C>A	NP_009225.1:p.Ala1611Asp
NM_007297.3:c.4691C>A	NP_009228.2:p.Ala1564Asp
NM_007298.3:c.1520C>A	NP_009229.2:p.Ala507Asp
NM_007299.3:c.1520C>A	NP_009230.2:p.Ala507Asp
NM_007300.3:c.4895C>A	NP_009231.2:p.Ala1632Asp
NR_027676.1:n.4968C>A
NM_007294.4:c.4832C>A MANE Select	NP_009225.1:p.Ala1611Asp
NM_007297.4:c.4691C>A	NP_009228.2:p.Ala1564Asp
NM_007299.4:c.1520C>A	NP_009230.2:p.Ala507Asp
NM_007300.4:c.4895C>A	NP_009231.2:p.Ala1632Asp
NR_027676.2:n.5009C>A