Canonical Allele Identifier: CA16620425

Gene: BRCA1

Linked Data

• ClinVar Variation Id: 418999
• ClinVar RCV Id: RCV000481460 ; RCV000584270 ; RCV000661132 ; RCV000800768
• dbSNP Id: rs1064793577
• MyVariant Identifiers: chr17:g.41228597del (hg19) ; chr17:g.43076580del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43076580del , CM000679.2:g.43076580del	GRCh38
NC_000017.10:g.41228597del , CM000679.1:g.41228597del	GRCh37
NC_000017.9:g.38482123del	NCBI36
NG_005905.2:g.141404del , LRG_292:g.141404del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461574.2:c.4389del	ENSP00000417241.2:p.Ile1464Ter
ENST00000470026.6:c.4392del	ENSP00000419274.2:p.Ile1465Ter
ENST00000473961.6:c.4266del	ENSP00000420201.2:p.Ile1423Ter
ENST00000476777.6:c.4386del	ENSP00000417554.2:p.Ile1463Ter
ENST00000477152.6:c.4314del	ENSP00000419988.2:p.Ile1439Ter
ENST00000478531.6:c.1080del	ENSP00000420412.2:p.Ile361Ter
ENST00000489037.2:c.4314del	ENSP00000420781.2:p.Ile1439Ter
ENST00000493919.6:c.942del	ENSP00000418819.2:p.Ile315Ter
ENST00000494123.6:c.4392del	ENSP00000419103.2:p.Ile1465Ter
ENST00000497488.2:c.3504del	ENSP00000418986.2:p.Ile1169Ter
ENST00000618469.2:c.4392del	ENSP00000478114.2:p.Ile1465Ter
ENST00000634433.2:c.4269del	ENSP00000489431.2:p.Ile1424Ter
ENST00000644379.2:c.4458del	ENSP00000496570.2:p.Ile1487Ter
ENST00000644555.2:c.942del	ENSP00000494614.2:p.Ile315Ter
ENST00000652672.2:c.4251del	ENSP00000498906.2:p.Ile1418Ter
ENST00000484087.6:c.954del	ENSP00000419481.2:p.Ile319Ter
ENST00000700182.1:c.999del	ENSP00000514849.1:p.Ile334Ter
ENST00000357654.9:c.4392del MANE Select	ENSP00000350283.3:p.Ile1465Ter
ENST00000471181.7:c.4455del	ENSP00000418960.2:p.Ile1486Ter
ENST00000644379.1:c.779del
ENST00000352993.7:c.966del	ENSP00000312236.5:p.Ile323Ter
ENST00000357654.7:c.4392del	ENSP00000350283.3:p.Ile1465Ter
ENST00000461221.5:c.*4175del	ENSP00000418548.1:n.*4175del
ENST00000461574.1:c.683del
ENST00000468300.5:c.1080del	ENSP00000417148.1:p.Ile361Ter
ENST00000471181.6:c.4455del	ENSP00000418960.2:p.Ile1486Ter
ENST00000478531.5:c.1080del	ENSP00000420412.1:p.Ile361Ter
ENST00000484087.5:c.705del	ENSP00000419481.1:p.Ile236Ter
ENST00000487825.5:c.708del	ENSP00000418212.1:p.Ile237Ter
ENST00000491747.6:c.1080del	ENSP00000420705.2:p.Ile361Ter
ENST00000493795.5:c.4251del	ENSP00000418775.1:p.Ile1418Ter
ENST00000493919.5:c.942del	ENSP00000418819.1:p.Ile315Ter
ENST00000586385.5:c.5-12629del	ENSP00000465818.1:n.5-12629del
ENST00000591534.5:c.-43-2059del	ENSP00000467329.1:n.-43-2059del
ENST00000591849.5:c.-98-26390del	ENSP00000465347.1:n.-98-26390del
ENST00000621897.1:n.283del
NM_007294.3:c.4392del , LRG_292t1:c.4392del	NP_009225.1:p.Ile1465Ter
NM_007297.3:c.4251del	NP_009228.2:p.Ile1418Ter
NM_007298.3:c.1080del	NP_009229.2:p.Ile361Ter
NM_007299.3:c.1080del	NP_009230.2:p.Ile361Ter
NM_007300.3:c.4455del	NP_009231.2:p.Ile1486Ter
NR_027676.1:n.4528del
NM_007294.4:c.4392del MANE Select	NP_009225.1:p.Ile1465Ter
NM_007297.4:c.4251del	NP_009228.2:p.Ile1418Ter
NM_007299.4:c.1080del	NP_009230.2:p.Ile361Ter
NM_007300.4:c.4455del	NP_009231.2:p.Ile1486Ter
NR_027676.2:n.4569del