Canonical Allele Identifier: CA2638062103

Gene: BRCA1

Linked Data

• gnomAD v4: 17-43067774-ATATGTTTACC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43067780_43067789del , CM000679.2:g.43067780_43067789del	GRCh38
NC_000017.10:g.41219797_41219806del , CM000679.1:g.41219797_41219806del	GRCh37
NC_000017.9:g.38473323_38473332del	NCBI36
NG_005905.2:g.150200_150209del , LRG_292:g.150200_150209del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461574.2:c.4984-89_4984-80del	ENSP00000417241.2:n.4984-89_4984-80del
ENST00000470026.6:c.4987-89_4987-80del	ENSP00000419274.2:n.4987-89_4987-80del
ENST00000473961.6:c.4861-89_4861-80del	ENSP00000420201.2:n.4861-89_4861-80del
ENST00000476777.6:c.4981-89_4981-80del	ENSP00000417554.2:n.4981-89_4981-80del
ENST00000477152.6:c.4909-89_4909-80del	ENSP00000419988.2:n.4909-89_4909-80del
ENST00000478531.6:c.1675-89_1675-80del	ENSP00000420412.2:n.1675-89_1675-80del
ENST00000489037.2:c.4909-89_4909-80del	ENSP00000420781.2:n.4909-89_4909-80del
ENST00000493919.6:c.1537-89_1537-80del	ENSP00000418819.2:n.1537-89_1537-80del
ENST00000494123.6:c.4987-89_4987-80del	ENSP00000419103.2:n.4987-89_4987-80del
ENST00000497488.2:c.4099-89_4099-80del	ENSP00000418986.2:n.4099-89_4099-80del
ENST00000618469.2:c.4987-89_4987-80del	ENSP00000478114.2:n.4987-89_4987-80del
ENST00000634433.2:c.4864-89_4864-80del	ENSP00000489431.2:n.4864-89_4864-80del
ENST00000644379.2:c.5053-89_5053-80del	ENSP00000496570.2:n.5053-89_5053-80del
ENST00000644555.2:c.1537-89_1537-80del	ENSP00000494614.2:n.1537-89_1537-80del
ENST00000652672.2:c.4846-89_4846-80del	ENSP00000498906.2:n.4846-89_4846-80del
ENST00000484087.6:c.1549-89_1549-80del	ENSP00000419481.2:n.1549-89_1549-80del
ENST00000357654.9:c.4987-89_4987-80del MANE Select	ENSP00000350283.3:n.4987-89_4987-80del
ENST00000471181.7:c.5050-89_5050-80del	ENSP00000418960.2:n.5050-89_5050-80del
ENST00000644379.1:c.1374-89_1374-80del
ENST00000352993.7:c.1561-89_1561-80del	ENSP00000312236.5:n.1561-89_1561-80del
ENST00000357654.7:c.4987-89_4987-80del	ENSP00000350283.3:n.4987-89_4987-80del
ENST00000461221.5:c.*4770-89_*4770-80del	ENSP00000418548.1:n.*4770-89_*4770-80del
ENST00000468300.5:c.1675-89_1675-80del	ENSP00000417148.1:n.1675-89_1675-80del
ENST00000471181.6:c.5050-89_5050-80del	ENSP00000418960.2:n.5050-89_5050-80del
ENST00000472490.1:n.140-89_140-80del
ENST00000478531.5:c.1675-89_1675-80del	ENSP00000420412.1:n.1675-89_1675-80del
ENST00000484087.5:c.1300-89_1300-80del	ENSP00000419481.1:n.1300-89_1300-80del
ENST00000491747.6:c.1675-89_1675-80del	ENSP00000420705.2:n.1675-89_1675-80del
ENST00000493795.5:c.4846-89_4846-80del	ENSP00000418775.1:n.4846-89_4846-80del
ENST00000493919.5:c.1537-89_1537-80del	ENSP00000418819.1:n.1537-89_1537-80del
ENST00000586385.5:c.5-3833_5-3824del	ENSP00000465818.1:n.5-3833_5-3824del
ENST00000591534.5:c.460-89_460-80del	ENSP00000467329.1:n.460-89_460-80del
ENST00000591849.5:c.-98-17594_-98-17585del	ENSP00000465347.1:n.-98-17594_-98-17585del
NM_007294.3:c.4987-89_4987-80del , LRG_292t1:c.4987-89_4987-80del	NP_009225.1:n.4987-89_4987-80del
NM_007297.3:c.4846-89_4846-80del	NP_009228.2:n.4846-89_4846-80del
NM_007298.3:c.1675-89_1675-80del	NP_009229.2:n.1675-89_1675-80del
NM_007299.3:c.1675-89_1675-80del	NP_009230.2:n.1675-89_1675-80del
NM_007300.3:c.5050-89_5050-80del	NP_009231.2:n.5050-89_5050-80del
NR_027676.1:n.5123-89_5123-80del
NM_007294.4:c.4987-89_4987-80del MANE Select	NP_009225.1:n.4987-89_4987-80del
NM_007297.4:c.4846-89_4846-80del	NP_009228.2:n.4846-89_4846-80del
NM_007299.4:c.1675-89_1675-80del	NP_009230.2:n.1675-89_1675-80del
NM_007300.4:c.5050-89_5050-80del	NP_009231.2:n.5050-89_5050-80del
NR_027676.2:n.5164-89_5164-80del