Canonical Allele Identifier: CA10591241

Gene: BRCA1

Linked Data

• ClinVar Variation Id: 627968
• ClinVar RCV Id: RCV000772239 ; RCV001050456 ; RCV001076083
• dbSNP Id: rs1567769155
• MyVariant Identifiers: chr17:g.41215891A>C (hg19) ; chr17:g.43063874A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43063874A>C , CM000679.2:g.43063874A>C	GRCh38
NC_000017.10:g.41215891A>C , CM000679.1:g.41215891A>C	GRCh37
NC_000017.9:g.38469417A>C	NCBI36
NG_005905.2:g.154110T>G , LRG_292:g.154110T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000461574.2:c.5149T>G	ENSP00000417241.2:p.Trp1717Gly
ENST00000470026.6:c.5152T>G	ENSP00000419274.2:p.Trp1718Gly
ENST00000473961.6:c.5026T>G	ENSP00000420201.2:p.Trp1676Gly
ENST00000476777.6:c.5146T>G	ENSP00000417554.2:p.Trp1716Gly
ENST00000477152.6:c.5074T>G	ENSP00000419988.2:p.Trp1692Gly
ENST00000478531.6:c.1840T>G	ENSP00000420412.2:p.Trp614Gly
ENST00000489037.2:c.5074T>G	ENSP00000420781.2:p.Trp1692Gly
ENST00000493919.6:c.1702T>G	ENSP00000418819.2:p.Trp568Gly
ENST00000494123.6:c.5152T>G	ENSP00000419103.2:p.Trp1718Gly
ENST00000497488.2:c.4264T>G	ENSP00000418986.2:p.Trp1422Gly
ENST00000618469.2:c.5152T>G	ENSP00000478114.2:p.Trp1718Gly
ENST00000634433.2:c.5029T>G	ENSP00000489431.2:p.Trp1677Gly
ENST00000644379.2:c.5218T>G	ENSP00000496570.2:p.Trp1740Gly
ENST00000644555.2:c.1702T>G	ENSP00000494614.2:p.Trp568Gly
ENST00000652672.2:c.5011T>G	ENSP00000498906.2:p.Trp1671Gly
ENST00000484087.6:c.1714T>G	ENSP00000419481.2:p.Trp572Gly
ENST00000357654.9:c.5152T>G MANE Select	ENSP00000350283.3:p.Trp1718Gly
ENST00000471181.7:c.5215T>G	ENSP00000418960.2:p.Trp1739Gly
ENST00000644379.1:c.1539T>G
ENST00000352993.7:c.1726T>G	ENSP00000312236.5:p.Trp576Gly
ENST00000357654.7:c.5152T>G	ENSP00000350283.3:p.Trp1718Gly
ENST00000461221.5:c.*4935T>G	ENSP00000418548.1:n.*4935T>G
ENST00000468300.5:c.1840T>G	ENSP00000417148.1:p.Trp614Gly
ENST00000471181.6:c.5215T>G	ENSP00000418960.2:p.Trp1739Gly
ENST00000478531.5:c.1840T>G	ENSP00000420412.1:p.Trp614Gly
ENST00000484087.5:c.1465T>G	ENSP00000419481.1:p.Trp489Gly
ENST00000491747.6:c.1840T>G	ENSP00000420705.2:p.Trp614Gly
ENST00000493795.5:c.5011T>G	ENSP00000418775.1:p.Trp1671Gly
ENST00000493919.5:c.1702T>G	ENSP00000418819.1:p.Trp568Gly
ENST00000586385.5:c.82T>G	ENSP00000465818.1:p.Trp28Gly
ENST00000591534.5:c.625T>G	ENSP00000467329.1:p.Trp209Gly
ENST00000591849.5:c.-98-13684T>G	ENSP00000465347.1:n.-98-13684T>G
NM_007294.3:c.5152T>G , LRG_292t1:c.5152T>G	NP_009225.1:p.Trp1718Gly
NM_007297.3:c.5011T>G	NP_009228.2:p.Trp1671Gly
NM_007298.3:c.1840T>G	NP_009229.2:p.Trp614Gly
NM_007299.3:c.1840T>G	NP_009230.2:p.Trp614Gly
NM_007300.3:c.5215T>G	NP_009231.2:p.Trp1739Gly
NR_027676.1:n.5288T>G
NM_007294.4:c.5152T>G MANE Select	NP_009225.1:p.Trp1718Gly
NM_007297.4:c.5011T>G	NP_009228.2:p.Trp1671Gly
NM_007299.4:c.1840T>G	NP_009230.2:p.Trp614Gly
NM_007300.4:c.5215T>G	NP_009231.2:p.Trp1739Gly
NR_027676.2:n.5329T>G