Canonical Allele Identifier: CA10589739

Gene: BRCA1

Linked Data

• ClinVar Variation Id: 266386
• ClinVar RCV Id: RCV000257158 ; RCV000637420
• dbSNP Id: rs886040145
• MyVariant Identifiers: chr17:g.41243977del (hg19) ; chr17:g.43091960del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43091960del , CM000679.2:g.43091960del	GRCh38
NC_000017.10:g.41243977del , CM000679.1:g.41243977del	GRCh37
NC_000017.9:g.38497503del	NCBI36
NG_005905.2:g.126024del , LRG_292:g.126024del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354071.8:n.3635del
ENST00000461574.2:c.3571del	ENSP00000417241.2:p.Ser1191AlafsTer19
ENST00000470026.6:c.3571del	ENSP00000419274.2:p.Ser1191AlafsTer19
ENST00000473961.6:c.3445del	ENSP00000420201.2:p.Ser1149AlafsTer19
ENST00000476777.6:c.3568del	ENSP00000417554.2:p.Ser1190AlafsTer19
ENST00000477152.6:c.3493del	ENSP00000419988.2:p.Ser1165AlafsTer19
ENST00000478531.6:c.785-928del	ENSP00000420412.2:n.785-928del
ENST00000489037.2:c.3493del	ENSP00000420781.2:p.Ser1165AlafsTer19
ENST00000493919.6:c.647-928del	ENSP00000418819.2:n.647-928del
ENST00000494123.6:c.3571del	ENSP00000419103.2:p.Ser1191AlafsTer19
ENST00000497488.2:c.2683del	ENSP00000418986.2:p.Ser895AlafsTer19
ENST00000618469.2:c.3571del	ENSP00000478114.2:p.Ser1191AlafsTer19
ENST00000634433.2:c.3448del	ENSP00000489431.2:p.Ser1150AlafsTer19
ENST00000644379.2:c.3571del	ENSP00000496570.2:p.Ser1191AlafsTer19
ENST00000644555.2:c.647-928del	ENSP00000494614.2:n.647-928del
ENST00000652672.2:c.3430del	ENSP00000498906.2:p.Ser1144AlafsTer19
ENST00000484087.6:c.665-928del	ENSP00000419481.2:n.665-928del
ENST00000700182.1:c.707-928del	ENSP00000514849.1:n.707-928del
ENST00000357654.9:c.3571del MANE Select	ENSP00000350283.3:p.Ser1191AlafsTer19
ENST00000471181.7:c.3571del	ENSP00000418960.2:p.Ser1191AlafsTer19
ENST00000352993.7:c.671-928del	ENSP00000312236.5:n.671-928del
ENST00000354071.7:c.3571del	ENSP00000326002.7:p.Ser1191AlafsTer19
ENST00000357654.7:c.3571del	ENSP00000350283.3:p.Ser1191AlafsTer19
ENST00000461221.5:c.*3354del	ENSP00000418548.1:n.*3354del
ENST00000468300.5:c.788-928del	ENSP00000417148.1:n.788-928del
ENST00000471181.6:c.3571del	ENSP00000418960.2:p.Ser1191AlafsTer19
ENST00000478531.5:c.785-928del	ENSP00000420412.1:n.785-928del
ENST00000484087.5:c.410-928del	ENSP00000419481.1:n.410-928del
ENST00000487825.5:c.413-928del	ENSP00000418212.1:n.413-928del
ENST00000491747.6:c.788-928del	ENSP00000420705.2:n.788-928del
ENST00000493795.5:c.3430del	ENSP00000418775.1:p.Ser1144AlafsTer19
ENST00000493919.5:c.647-928del	ENSP00000418819.1:n.647-928del
ENST00000586385.5:c.5-28009del	ENSP00000465818.1:n.5-28009del
ENST00000591534.5:c.-43-17439del	ENSP00000467329.1:n.-43-17439del
ENST00000591849.5:c.-99+33311del	ENSP00000465347.1:n.-99+33311del
NM_007294.3:c.3571del , LRG_292t1:c.3571del	NP_009225.1:p.Ser1191AlafsTer19
NM_007297.3:c.3430del	NP_009228.2:p.Ser1144AlafsTer19
NM_007298.3:c.788-928del	NP_009229.2:n.788-928del
NM_007299.3:c.788-928del	NP_009230.2:n.788-928del
NM_007300.3:c.3571del	NP_009231.2:p.Ser1191AlafsTer19
NR_027676.1:n.3707del
NM_007294.4:c.3571del MANE Select	NP_009225.1:p.Ser1191AlafsTer19
NM_007297.4:c.3430del	NP_009228.2:p.Ser1144AlafsTer19
NM_007299.4:c.788-928del	NP_009230.2:n.788-928del
NM_007300.4:c.3571del	NP_009231.2:p.Ser1191AlafsTer19
NR_027676.2:n.3748del