Canonical Allele Identifier: CA001509

Gene: BRCA1

Linked Data

• ClinVar Variation Id: 54515
• ClinVar RCV Id: RCV000111808
• dbSNP Id: rs80357602
• MyVariant Identifiers: chr17:g.41245294_41245295del (hg19) ; chr17:g.43093277_43093278del (hg38)
• PubMed: PMID:10874312

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43093278_43093279del , CM000679.2:g.43093278_43093279del	GRCh38
NC_000017.10:g.41245295_41245296del , CM000679.1:g.41245295_41245296del	GRCh37
NC_000017.9:g.38498821_38498822del	NCBI36
NG_005905.2:g.124706_124707del , LRG_292:g.124706_124707del

Transcript Alleles

HGVS	Amino-acid change
ENST00000354071.8:n.2317_2318del
ENST00000461574.2:c.2253_2254del	ENSP00000417241.2:p.Met751IlefsTer10
ENST00000470026.6:c.2253_2254del	ENSP00000419274.2:p.Met751IlefsTer10
ENST00000473961.6:c.2127_2128del	ENSP00000420201.2:p.Met709IlefsTer10
ENST00000476777.6:c.2250_2251del	ENSP00000417554.2:p.Met750IlefsTer10
ENST00000477152.6:c.2175_2176del	ENSP00000419988.2:p.Met725IlefsTer10
ENST00000478531.6:c.784+1466_784+1467del	ENSP00000420412.2:n.784+1466_784+1467del
ENST00000489037.2:c.2175_2176del	ENSP00000420781.2:p.Met725IlefsTer10
ENST00000493919.6:c.646+1466_646+1467del	ENSP00000418819.2:n.646+1466_646+1467del
ENST00000494123.6:c.2253_2254del	ENSP00000419103.2:p.Met751IlefsTer10
ENST00000497488.2:c.1365_1366del	ENSP00000418986.2:p.Met455IlefsTer10
ENST00000618469.2:c.2253_2254del	ENSP00000478114.2:p.Met751IlefsTer10
ENST00000634433.2:c.2130_2131del	ENSP00000489431.2:p.Met710IlefsTer10
ENST00000644379.2:c.2253_2254del	ENSP00000496570.2:p.Met751IlefsTer10
ENST00000644555.2:c.646+1466_646+1467del	ENSP00000494614.2:n.646+1466_646+1467del
ENST00000652672.2:c.2112_2113del	ENSP00000498906.2:p.Met704IlefsTer10
ENST00000484087.6:c.664+1466_664+1467del	ENSP00000419481.2:n.664+1466_664+1467del
ENST00000700182.1:c.706+1466_706+1467del	ENSP00000514849.1:n.706+1466_706+1467del
ENST00000357654.9:c.2253_2254del MANE Select	ENSP00000350283.3:p.Met751IlefsTer10
ENST00000471181.7:c.2253_2254del	ENSP00000418960.2:p.Met751IlefsTer10
ENST00000352993.7:c.671-2246_671-2245del	ENSP00000312236.5:n.671-2246_671-2245del
ENST00000354071.7:c.2253_2254del	ENSP00000326002.7:p.Met751IlefsTer10
ENST00000357654.7:c.2253_2254del	ENSP00000350283.3:p.Met751IlefsTer10
ENST00000461221.5:c.*2036_*2037del	ENSP00000418548.1:n.*2036_*2037del
ENST00000468300.5:c.787+1466_787+1467del	ENSP00000417148.1:n.787+1466_787+1467del
ENST00000471181.6:c.2253_2254del	ENSP00000418960.2:p.Met751IlefsTer10
ENST00000478531.5:c.784+1466_784+1467del	ENSP00000420412.1:n.784+1466_784+1467del
ENST00000484087.5:c.409+1466_409+1467del	ENSP00000419481.1:n.409+1466_409+1467del
ENST00000487825.5:c.412+1466_412+1467del	ENSP00000418212.1:n.412+1466_412+1467del
ENST00000491747.6:c.787+1466_787+1467del	ENSP00000420705.2:n.787+1466_787+1467del
ENST00000493795.5:c.2112_2113del	ENSP00000418775.1:p.Met704IlefsTer10
ENST00000493919.5:c.646+1466_646+1467del	ENSP00000418819.1:n.646+1466_646+1467del
ENST00000586385.5:c.5-29327_5-29326del	ENSP00000465818.1:n.5-29327_5-29326del
ENST00000591534.5:c.-43-18757_-43-18756del	ENSP00000467329.1:n.-43-18757_-43-18756del
ENST00000591849.5:c.-99+31993_-99+31994del	ENSP00000465347.1:n.-99+31993_-99+31994del
ENST00000634433.1:c.2130_2131del	ENSP00000489431.1:p.Met710IlefsTer10
NM_007294.3:c.2253_2254del , LRG_292t1:c.2253_2254del	NP_009225.1:p.Met751IlefsTer10
NM_007297.3:c.2112_2113del	NP_009228.2:p.Met704IlefsTer10
NM_007298.3:c.787+1466_787+1467del	NP_009229.2:n.787+1466_787+1467del
NM_007299.3:c.787+1466_787+1467del	NP_009230.2:n.787+1466_787+1467del
NM_007300.3:c.2253_2254del	NP_009231.2:p.Met751IlefsTer10
NR_027676.1:n.2389_2390del
NM_007294.4:c.2253_2254del MANE Select	NP_009225.1:p.Met751IlefsTer10
NM_007297.4:c.2112_2113del	NP_009228.2:p.Met704IlefsTer10
NM_007299.4:c.787+1466_787+1467del	NP_009230.2:n.787+1466_787+1467del
NM_007300.4:c.2253_2254del	NP_009231.2:p.Met751IlefsTer10
NR_027676.2:n.2430_2431del