Canonical Allele Identifier: CA003452

Gene: BRCA1

Linked Data

• ClinVar Variation Id: 37656
• ClinVar RCV Id: RCV000031237 ; RCV000048915 ; RCV000218342 ; RCV001284552
• dbSNP Id: rs80357463
• MyVariant Identifiers: chr17:g.41203115A>C (hg19) ; chr17:g.43051098A>C (hg38)
• PubMed: PMID:17308087 ; PMID:21990134

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43051098A>C , CM000679.2:g.43051098A>C	GRCh38
NC_000017.10:g.41203115A>C , CM000679.1:g.41203115A>C	GRCh37
NC_000017.9:g.38456641A>C	NCBI36
NG_005905.2:g.166886T>G , LRG_292:g.166886T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461574.2:c.5294T>G	ENSP00000417241.2:p.Ile1765Ser
ENST00000470026.6:c.5297T>G	ENSP00000419274.2:p.Ile1766Ser
ENST00000473961.6:c.5171T>G	ENSP00000420201.2:p.Ile1724Ser
ENST00000476777.6:c.5291T>G	ENSP00000417554.2:p.Ile1764Ser
ENST00000477152.6:c.5219T>G	ENSP00000419988.2:p.Ile1740Ser
ENST00000478531.6:c.1985T>G	ENSP00000420412.2:p.Ile662Ser
ENST00000489037.2:c.5219T>G	ENSP00000420781.2:p.Ile1740Ser
ENST00000493919.6:c.1847T>G	ENSP00000418819.2:p.Ile616Ser
ENST00000494123.6:c.5297T>G	ENSP00000419103.2:p.Ile1766Ser
ENST00000497488.2:c.4409T>G	ENSP00000418986.2:p.Ile1470Ser
ENST00000618469.2:c.5297T>G	ENSP00000478114.2:p.Ile1766Ser
ENST00000634433.2:c.5174T>G	ENSP00000489431.2:p.Ile1725Ser
ENST00000644379.2:c.5363T>G	ENSP00000496570.2:p.Ile1788Ser
ENST00000644555.2:c.1847T>G	ENSP00000494614.2:p.Ile616Ser
ENST00000652672.2:c.5156T>G	ENSP00000498906.2:p.Ile1719Ser
ENST00000484087.6:c.1859T>G	ENSP00000419481.2:p.Ile620Ser
ENST00000357654.9:c.5297T>G MANE Select	ENSP00000350283.3:p.Ile1766Ser
ENST00000471181.7:c.5360T>G	ENSP00000418960.2:p.Ile1787Ser
ENST00000644379.1:c.1684T>G
ENST00000352993.7:c.1871T>G	ENSP00000312236.5:p.Ile624Ser
ENST00000357654.7:c.5297T>G	ENSP00000350283.3:p.Ile1766Ser
ENST00000461221.5:c.*5080T>G	ENSP00000418548.1:n.*5080T>G
ENST00000468300.5:c.1985T>G	ENSP00000417148.1:p.Ile662Ser
ENST00000471181.6:c.5360T>G	ENSP00000418960.2:p.Ile1787Ser
ENST00000491747.6:c.1985T>G	ENSP00000420705.2:p.Ile662Ser
ENST00000493795.5:c.5156T>G	ENSP00000418775.1:p.Ile1719Ser
ENST00000586385.5:c.227T>G	ENSP00000465818.1:p.Ile76Ser
ENST00000591534.5:c.770T>G	ENSP00000467329.1:p.Ile257Ser
ENST00000591849.5:c.-98-908T>G	ENSP00000465347.1:n.-98-908T>G
NM_007294.3:c.5297T>G , LRG_292t1:c.5297T>G	NP_009225.1:p.Ile1766Ser
NM_007297.3:c.5156T>G	NP_009228.2:p.Ile1719Ser
NM_007298.3:c.1985T>G	NP_009229.2:p.Ile662Ser
NM_007299.3:c.1985T>G	NP_009230.2:p.Ile662Ser
NM_007300.3:c.5360T>G	NP_009231.2:p.Ile1787Ser
NR_027676.1:n.5433T>G
NM_007294.4:c.5297T>G MANE Select	NP_009225.1:p.Ile1766Ser
NM_007297.4:c.5156T>G	NP_009228.2:p.Ile1719Ser
NM_007299.4:c.1985T>G	NP_009230.2:p.Ile662Ser
NM_007300.4:c.5360T>G	NP_009231.2:p.Ile1787Ser
NR_027676.2:n.5474T>G