Canonical Allele Identifier: CA656358873

Gene: BRCA1

Linked Data

• COSMIC: COSN25687353

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43067429_43067439del , CM000679.2:g.43067429_43067439del	GRCh38
NC_000017.10:g.41219446_41219456del , CM000679.1:g.41219446_41219456del	GRCh37
NC_000017.9:g.38472972_38472982del	NCBI36
NG_005905.2:g.150545_150555del , LRG_292:g.150545_150555del

Transcript Alleles

HGVS	Amino-acid change
ENST00000461574.2:c.5071+169_5071+179del	ENSP00000417241.2:n.5071+169_5071+179del
ENST00000470026.6:c.5074+169_5074+179del	ENSP00000419274.2:n.5074+169_5074+179del
ENST00000473961.6:c.4948+169_4948+179del	ENSP00000420201.2:n.4948+169_4948+179del
ENST00000476777.6:c.5068+169_5068+179del	ENSP00000417554.2:n.5068+169_5068+179del
ENST00000477152.6:c.4996+169_4996+179del	ENSP00000419988.2:n.4996+169_4996+179del
ENST00000478531.6:c.1762+169_1762+179del	ENSP00000420412.2:n.1762+169_1762+179del
ENST00000489037.2:c.4996+169_4996+179del	ENSP00000420781.2:n.4996+169_4996+179del
ENST00000493919.6:c.1624+169_1624+179del	ENSP00000418819.2:n.1624+169_1624+179del
ENST00000494123.6:c.5074+169_5074+179del	ENSP00000419103.2:n.5074+169_5074+179del
ENST00000497488.2:c.4186+169_4186+179del	ENSP00000418986.2:n.4186+169_4186+179del
ENST00000618469.2:c.5074+169_5074+179del	ENSP00000478114.2:n.5074+169_5074+179del
ENST00000634433.2:c.4951+169_4951+179del	ENSP00000489431.2:n.4951+169_4951+179del
ENST00000644379.2:c.5140+169_5140+179del	ENSP00000496570.2:n.5140+169_5140+179del
ENST00000644555.2:c.1624+169_1624+179del	ENSP00000494614.2:n.1624+169_1624+179del
ENST00000652672.2:c.4933+169_4933+179del	ENSP00000498906.2:n.4933+169_4933+179del
ENST00000484087.6:c.1636+169_1636+179del	ENSP00000419481.2:n.1636+169_1636+179del
ENST00000357654.9:c.5074+169_5074+179del MANE Select	ENSP00000350283.3:n.5074+169_5074+179del
ENST00000471181.7:c.5137+169_5137+179del	ENSP00000418960.2:n.5137+169_5137+179del
ENST00000644379.1:c.1461+169_1461+179del
ENST00000352993.7:c.1648+169_1648+179del	ENSP00000312236.5:n.1648+169_1648+179del
ENST00000357654.7:c.5074+169_5074+179del	ENSP00000350283.3:n.5074+169_5074+179del
ENST00000461221.5:c.*4857+169_*4857+179del	ENSP00000418548.1:n.*4857+169_*4857+179de...
ENST00000468300.5:c.1762+169_1762+179del	ENSP00000417148.1:n.1762+169_1762+179del
ENST00000471181.6:c.5137+169_5137+179del	ENSP00000418960.2:n.5137+169_5137+179del
ENST00000472490.1:n.396_406del
ENST00000478531.5:c.1762+169_1762+179del	ENSP00000420412.1:n.1762+169_1762+179del
ENST00000484087.5:c.1387+169_1387+179del	ENSP00000419481.1:n.1387+169_1387+179del
ENST00000491747.6:c.1762+169_1762+179del	ENSP00000420705.2:n.1762+169_1762+179del
ENST00000493795.5:c.4933+169_4933+179del	ENSP00000418775.1:n.4933+169_4933+179del
ENST00000493919.5:c.1624+169_1624+179del	ENSP00000418819.1:n.1624+169_1624+179del
ENST00000586385.5:c.5-3488_5-3478del	ENSP00000465818.1:n.5-3488_5-3478del
ENST00000591534.5:c.547+169_547+179del	ENSP00000467329.1:n.547+169_547+179del
ENST00000591849.5:c.-98-17249_-98-17239del	ENSP00000465347.1:n.-98-17249_-98-17239de...
NM_007294.3:c.5074+169_5074+179del , LRG_292t1:c.5074+169_5074+179del	NP_009225.1:n.5074+169_5074+179del
NM_007297.3:c.4933+169_4933+179del	NP_009228.2:n.4933+169_4933+179del
NM_007298.3:c.1762+169_1762+179del	NP_009229.2:n.1762+169_1762+179del
NM_007299.3:c.1762+169_1762+179del	NP_009230.2:n.1762+169_1762+179del
NM_007300.3:c.5137+169_5137+179del	NP_009231.2:n.5137+169_5137+179del
NR_027676.1:n.5210+169_5210+179del
NM_007294.4:c.5074+169_5074+179del MANE Select	NP_009225.1:n.5074+169_5074+179del
NM_007297.4:c.4933+169_4933+179del	NP_009228.2:n.4933+169_4933+179del
NM_007299.4:c.1762+169_1762+179del	NP_009230.2:n.1762+169_1762+179del
NM_007300.4:c.5137+169_5137+179del	NP_009231.2:n.5137+169_5137+179del
NR_027676.2:n.5251+169_5251+179del