Canonical Allele Identifier: CA002684

Gene: BRCA1

Linked Data

• ClinVar Variation Id: 55128
• ClinVar RCV Id: RCV000077566 ; RCV001377523 ; RCV002326771 ; RCV002272045
• dbSNP Id: rs80358076
• MyVariant Identifiers: chr17:g.41242960C>A (hg19) ; chr17:g.43090943C>A (hg38)
• PubMed: PMID:19491284

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43090943C>A , CM000679.2:g.43090943C>A	GRCh38
NC_000017.10:g.41242960C>A , CM000679.1:g.41242960C>A	GRCh37
NC_000017.9:g.38496486C>A	NCBI36
NG_005905.2:g.127041G>T , LRG_292:g.127041G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461574.2:c.4185+1G>T	ENSP00000417241.2:n.4185+1G>T
ENST00000470026.6:c.4185+1G>T	ENSP00000419274.2:n.4185+1G>T
ENST00000473961.6:c.4059+1G>T	ENSP00000420201.2:n.4059+1G>T
ENST00000476777.6:c.4182+1G>T	ENSP00000417554.2:n.4182+1G>T
ENST00000477152.6:c.4107+1G>T	ENSP00000419988.2:n.4107+1G>T
ENST00000478531.6:c.873+1G>T	ENSP00000420412.2:n.873+1G>T
ENST00000489037.2:c.4107+1G>T	ENSP00000420781.2:n.4107+1G>T
ENST00000493919.6:c.735+1G>T	ENSP00000418819.2:n.735+1G>T
ENST00000494123.6:c.4185+1G>T	ENSP00000419103.2:n.4185+1G>T
ENST00000497488.2:c.3297+1G>T	ENSP00000418986.2:n.3297+1G>T
ENST00000618469.2:c.4185+1G>T	ENSP00000478114.2:n.4185+1G>T
ENST00000634433.2:c.4062+1G>T	ENSP00000489431.2:n.4062+1G>T
ENST00000644379.2:c.4185+1G>T	ENSP00000496570.2:n.4185+1G>T
ENST00000644555.2:c.735+1G>T	ENSP00000494614.2:n.735+1G>T
ENST00000652672.2:c.4044+1G>T	ENSP00000498906.2:n.4044+1G>T
ENST00000484087.6:c.753+1G>T	ENSP00000419481.2:n.753+1G>T
ENST00000700182.1:c.795+1G>T	ENSP00000514849.1:n.795+1G>T
ENST00000357654.9:c.4185+1G>T MANE Select	ENSP00000350283.3:n.4185+1G>T
ENST00000471181.7:c.4185+1G>T	ENSP00000418960.2:n.4185+1G>T
ENST00000644379.1:c.506+1G>T
ENST00000352993.7:c.759+1G>T	ENSP00000312236.5:n.759+1G>T
ENST00000357654.7:c.4185+1G>T	ENSP00000350283.3:n.4185+1G>T
ENST00000461221.5:c.*3968+1G>T	ENSP00000418548.1:n.*3968+1G>T
ENST00000461574.1:c.479+1G>T
ENST00000468300.5:c.876+1G>T	ENSP00000417148.1:n.876+1G>T
ENST00000471181.6:c.4185+1G>T	ENSP00000418960.2:n.4185+1G>T
ENST00000478531.5:c.873+1G>T	ENSP00000420412.1:n.873+1G>T
ENST00000484087.5:c.498+1G>T	ENSP00000419481.1:n.498+1G>T
ENST00000487825.5:c.501+1G>T	ENSP00000418212.1:n.501+1G>T
ENST00000491747.6:c.876+1G>T	ENSP00000420705.2:n.876+1G>T
ENST00000493795.5:c.4044+1G>T	ENSP00000418775.1:n.4044+1G>T
ENST00000493919.5:c.735+1G>T	ENSP00000418819.1:n.735+1G>T
ENST00000586385.5:c.5-26992G>T	ENSP00000465818.1:n.5-26992G>T
ENST00000591534.5:c.-43-16422G>T	ENSP00000467329.1:n.-43-16422G>T
ENST00000591849.5:c.-99+34328G>T	ENSP00000465347.1:n.-99+34328G>T
NM_007294.3:c.4185+1G>T , LRG_292t1:c.4185+1G>T	NP_009225.1:n.4185+1G>T
NM_007297.3:c.4044+1G>T	NP_009228.2:n.4044+1G>T
NM_007298.3:c.876+1G>T	NP_009229.2:n.876+1G>T
NM_007299.3:c.876+1G>T	NP_009230.2:n.876+1G>T
NM_007300.3:c.4185+1G>T	NP_009231.2:n.4185+1G>T
NR_027676.1:n.4321+1G>T
NM_007294.4:c.4185+1G>T MANE Select	NP_009225.1:n.4185+1G>T
NM_007297.4:c.4044+1G>T	NP_009228.2:n.4044+1G>T
NM_007299.4:c.876+1G>T	NP_009230.2:n.876+1G>T
NM_007300.4:c.4185+1G>T	NP_009231.2:n.4185+1G>T
NR_027676.2:n.4362+1G>T