Canonical Allele Identifier: CA772175762

Gene: BRCA1

Linked Data

• dbSNP Id: rs1368970765
• gnomAD v3: 17-43066820-T-TC
• gnomAD v4: 17-43066820-T-TC
• MyVariant Identifiers: chr17:g.41218837_41218838insC (hg19) ; chr17:g.43066820_43066821insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43066820_43066821insC , CM000679.2:g.43066820_43066821insC	GRCh38
NC_000017.10:g.41218837_41218838insC , CM000679.1:g.41218837_41218838insC	GRCh37
NC_000017.9:g.38472363_38472364insC	NCBI36
NG_005905.2:g.151163_151164insG , LRG_292:g.151163_151164insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461574.2:c.5071+787_5071+788insG	ENSP00000417241.2:n.5071+787_5071+788insG
ENST00000470026.6:c.5074+787_5074+788insG	ENSP00000419274.2:n.5074+787_5074+788insG
ENST00000473961.6:c.4948+787_4948+788insG	ENSP00000420201.2:n.4948+787_4948+788insG
ENST00000476777.6:c.5068+787_5068+788insG	ENSP00000417554.2:n.5068+787_5068+788insG
ENST00000477152.6:c.4996+787_4996+788insG	ENSP00000419988.2:n.4996+787_4996+788insG
ENST00000478531.6:c.1762+787_1762+788insG	ENSP00000420412.2:n.1762+787_1762+788insG
ENST00000489037.2:c.4996+787_4996+788insG	ENSP00000420781.2:n.4996+787_4996+788insG
ENST00000493919.6:c.1624+787_1624+788insG	ENSP00000418819.2:n.1624+787_1624+788insG
ENST00000494123.6:c.5074+787_5074+788insG	ENSP00000419103.2:n.5074+787_5074+788insG
ENST00000497488.2:c.4186+787_4186+788insG	ENSP00000418986.2:n.4186+787_4186+788insG
ENST00000618469.2:c.5074+787_5074+788insG	ENSP00000478114.2:n.5074+787_5074+788insG
ENST00000634433.2:c.4951+787_4951+788insG	ENSP00000489431.2:n.4951+787_4951+788insG
ENST00000644379.2:c.5140+787_5140+788insG	ENSP00000496570.2:n.5140+787_5140+788insG
ENST00000644555.2:c.1624+787_1624+788insG	ENSP00000494614.2:n.1624+787_1624+788insG
ENST00000652672.2:c.4933+787_4933+788insG	ENSP00000498906.2:n.4933+787_4933+788insG
ENST00000484087.6:c.1636+787_1636+788insG	ENSP00000419481.2:n.1636+787_1636+788insG
ENST00000357654.9:c.5074+787_5074+788insG MANE Select	ENSP00000350283.3:n.5074+787_5074+788insG
ENST00000471181.7:c.5137+787_5137+788insG	ENSP00000418960.2:n.5137+787_5137+788insG
ENST00000644379.1:c.1461+787_1461+788insG
ENST00000352993.7:c.1648+787_1648+788insG	ENSP00000312236.5:n.1648+787_1648+788insG
ENST00000357654.7:c.5074+787_5074+788insG	ENSP00000350283.3:n.5074+787_5074+788insG
ENST00000461221.5:c.*4857+787_*4857+788insG	ENSP00000418548.1:n.*4857+787_*4857+788insG
ENST00000468300.5:c.1762+787_1762+788insG	ENSP00000417148.1:n.1762+787_1762+788insG
ENST00000471181.6:c.5137+787_5137+788insG	ENSP00000418960.2:n.5137+787_5137+788insG
ENST00000478531.5:c.1762+787_1762+788insG	ENSP00000420412.1:n.1762+787_1762+788insG
ENST00000484087.5:c.1387+787_1387+788insG	ENSP00000419481.1:n.1387+787_1387+788insG
ENST00000491747.6:c.1762+787_1762+788insG	ENSP00000420705.2:n.1762+787_1762+788insG
ENST00000493795.5:c.4933+787_4933+788insG	ENSP00000418775.1:n.4933+787_4933+788insG
ENST00000493919.5:c.1624+787_1624+788insG	ENSP00000418819.1:n.1624+787_1624+788insG
ENST00000586385.5:c.5-2870_5-2869insG	ENSP00000465818.1:n.5-2870_5-2869insG
ENST00000591534.5:c.547+787_547+788insG	ENSP00000467329.1:n.547+787_547+788insG
ENST00000591849.5:c.-98-16631_-98-16630insG	ENSP00000465347.1:n.-98-16631_-98-16630insG
NM_007294.3:c.5074+787_5074+788insG , LRG_292t1:c.5074+787_5074+788insG	NP_009225.1:n.5074+787_5074+788insG
NM_007297.3:c.4933+787_4933+788insG	NP_009228.2:n.4933+787_4933+788insG
NM_007298.3:c.1762+787_1762+788insG	NP_009229.2:n.1762+787_1762+788insG
NM_007299.3:c.1762+787_1762+788insG	NP_009230.2:n.1762+787_1762+788insG
NM_007300.3:c.5137+787_5137+788insG	NP_009231.2:n.5137+787_5137+788insG
NR_027676.1:n.5210+787_5210+788insG
NM_007294.4:c.5074+787_5074+788insG MANE Select	NP_009225.1:n.5074+787_5074+788insG
NM_007297.4:c.4933+787_4933+788insG	NP_009228.2:n.4933+787_4933+788insG
NM_007299.4:c.1762+787_1762+788insG	NP_009230.2:n.1762+787_1762+788insG
NM_007300.4:c.5137+787_5137+788insG	NP_009231.2:n.5137+787_5137+788insG
NR_027676.2:n.5251+787_5251+788insG