Canonical Allele Identifier: CA2580093931

Gene: BRCA1

Linked Data

• ClinVar Variation Id: 1802914
• ClinVar RCV Id: RCV002466189
• gnomAD v4: 17-43063286-ATGAC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43063290_43063293del , CM000679.2:g.43063290_43063293del	GRCh38
NC_000017.10:g.41215307_41215310del , CM000679.1:g.41215307_41215310del	GRCh37
NC_000017.9:g.38468833_38468836del	NCBI36
NG_005905.2:g.154694_154697del , LRG_292:g.154694_154697del

Transcript Alleles

HGVS	Amino-acid change
ENST00000461574.2:c.5190+43_5190+46del	ENSP00000417241.2:n.5190+43_5190+46del
ENST00000470026.6:c.5193+43_5193+46del	ENSP00000419274.2:n.5193+43_5193+46del
ENST00000473961.6:c.5067+43_5067+46del	ENSP00000420201.2:n.5067+43_5067+46del
ENST00000476777.6:c.5187+43_5187+46del	ENSP00000417554.2:n.5187+43_5187+46del
ENST00000477152.6:c.5115+43_5115+46del	ENSP00000419988.2:n.5115+43_5115+46del
ENST00000478531.6:c.1881+43_1881+46del	ENSP00000420412.2:n.1881+43_1881+46del
ENST00000489037.2:c.5115+43_5115+46del	ENSP00000420781.2:n.5115+43_5115+46del
ENST00000493919.6:c.1743+43_1743+46del	ENSP00000418819.2:n.1743+43_1743+46del
ENST00000494123.6:c.5193+43_5193+46del	ENSP00000419103.2:n.5193+43_5193+46del
ENST00000497488.2:c.4305+43_4305+46del	ENSP00000418986.2:n.4305+43_4305+46del
ENST00000618469.2:c.5193+43_5193+46del	ENSP00000478114.2:n.5193+43_5193+46del
ENST00000634433.2:c.5070+43_5070+46del	ENSP00000489431.2:n.5070+43_5070+46del
ENST00000644379.2:c.5259+43_5259+46del	ENSP00000496570.2:n.5259+43_5259+46del
ENST00000644555.2:c.1743+43_1743+46del	ENSP00000494614.2:n.1743+43_1743+46del
ENST00000652672.2:c.5052+43_5052+46del	ENSP00000498906.2:n.5052+43_5052+46del
ENST00000484087.6:c.1755+43_1755+46del	ENSP00000419481.2:n.1755+43_1755+46del
ENST00000357654.9:c.5193+43_5193+46del MANE Select	ENSP00000350283.3:n.5193+43_5193+46del
ENST00000471181.7:c.5256+43_5256+46del	ENSP00000418960.2:n.5256+43_5256+46del
ENST00000644379.1:c.1580+43_1580+46del
ENST00000352993.7:c.1767+43_1767+46del	ENSP00000312236.5:n.1767+43_1767+46del
ENST00000357654.7:c.5193+43_5193+46del	ENSP00000350283.3:n.5193+43_5193+46del
ENST00000461221.5:c.*4976+43_*4976+46del	ENSP00000418548.1:n.*4976+43_*4976+46del
ENST00000468300.5:c.1881+43_1881+46del	ENSP00000417148.1:n.1881+43_1881+46del
ENST00000471181.6:c.5256+43_5256+46del	ENSP00000418960.2:n.5256+43_5256+46del
ENST00000491747.6:c.1881+43_1881+46del	ENSP00000420705.2:n.1881+43_1881+46del
ENST00000493795.5:c.5052+43_5052+46del	ENSP00000418775.1:n.5052+43_5052+46del
ENST00000586385.5:c.123+43_123+46del	ENSP00000465818.1:n.123+43_123+46del
ENST00000591534.5:c.666+43_666+46del	ENSP00000467329.1:n.666+43_666+46del
ENST00000591849.5:c.-98-13100_-98-13097del	ENSP00000465347.1:n.-98-13100_-98-13097del
NM_007294.3:c.5193+43_5193+46del , LRG_292t1:c.5193+43_5193+46del	NP_009225.1:n.5193+43_5193+46del
NM_007297.3:c.5052+43_5052+46del	NP_009228.2:n.5052+43_5052+46del
NM_007298.3:c.1881+43_1881+46del	NP_009229.2:n.1881+43_1881+46del
NM_007299.3:c.1881+43_1881+46del	NP_009230.2:n.1881+43_1881+46del
NM_007300.3:c.5256+43_5256+46del	NP_009231.2:n.5256+43_5256+46del
NR_027676.1:n.5329+43_5329+46del
NM_007294.4:c.5193+43_5193+46del MANE Select	NP_009225.1:n.5193+43_5193+46del
NM_007297.4:c.5052+43_5052+46del	NP_009228.2:n.5052+43_5052+46del
NM_007299.4:c.1881+43_1881+46del	NP_009230.2:n.1881+43_1881+46del
NM_007300.4:c.5256+43_5256+46del	NP_009231.2:n.5256+43_5256+46del
NR_027676.2:n.5370+43_5370+46del