Canonical Allele Identifier: CA2260770863
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43066812_43066825delinsCTTTTTTTTTTTTT , CM000679.2:g.43066812_43066825delinsCTTTTTTTTTTTTT GRCh38
NC_000017.10:g.41218829_41218842delinsCTTTTTTTTTTTTT , CM000679.1:g.41218829_41218842delinsCTTTTTTTTTTTTT GRCh37
NC_000017.9:g.38472355_38472368delinsCTTTTTTTTTTTTT NCBI36
NG_005905.2:g.151159_151172delinsAAAAAAAAAAAAAG , LRG_292:g.151159_151172delinsAAAAAAAAAAAAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000461574.2:c.5071+783_5071+796delinsAAAAAAAAAAAAAG ENSP00000417241.2:n.5071+783_5071+796delinsAAAAAAAAAAAAAG
ENST00000470026.6:c.5074+783_5074+796delinsAAAAAAAAAAAAAG ENSP00000419274.2:n.5074+783_5074+796delinsAAAAAAAAAAAAAG
ENST00000473961.6:c.4948+783_4948+796delinsAAAAAAAAAAAAAG ENSP00000420201.2:n.4948+783_4948+796delinsAAAAAAAAAAAAAG
ENST00000476777.6:c.5068+783_5068+796delinsAAAAAAAAAAAAAG ENSP00000417554.2:n.5068+783_5068+796delinsAAAAAAAAAAAAAG
ENST00000477152.6:c.4996+783_4996+796delinsAAAAAAAAAAAAAG ENSP00000419988.2:n.4996+783_4996+796delinsAAAAAAAAAAAAAG
ENST00000478531.6:c.1762+783_1762+796delinsAAAAAAAAAAAAAG ENSP00000420412.2:n.1762+783_1762+796delinsAAAAAAAAAAAAAG
ENST00000489037.2:c.4996+783_4996+796delinsAAAAAAAAAAAAAG ENSP00000420781.2:n.4996+783_4996+796delinsAAAAAAAAAAAAAG
ENST00000493919.6:c.1624+783_1624+796delinsAAAAAAAAAAAAAG ENSP00000418819.2:n.1624+783_1624+796delinsAAAAAAAAAAAAAG
ENST00000494123.6:c.5074+783_5074+796delinsAAAAAAAAAAAAAG ENSP00000419103.2:n.5074+783_5074+796delinsAAAAAAAAAAAAAG
ENST00000497488.2:c.4186+783_4186+796delinsAAAAAAAAAAAAAG ENSP00000418986.2:n.4186+783_4186+796delinsAAAAAAAAAAAAAG
ENST00000618469.2:c.5074+783_5074+796delinsAAAAAAAAAAAAAG ENSP00000478114.2:n.5074+783_5074+796delinsAAAAAAAAAAAAAG
ENST00000634433.2:c.4951+783_4951+796delinsAAAAAAAAAAAAAG ENSP00000489431.2:n.4951+783_4951+796delinsAAAAAAAAAAAAAG
ENST00000644379.2:c.5140+783_5140+796delinsAAAAAAAAAAAAAG ENSP00000496570.2:n.5140+783_5140+796delinsAAAAAAAAAAAAAG
ENST00000644555.2:c.1624+783_1624+796delinsAAAAAAAAAAAAAG ENSP00000494614.2:n.1624+783_1624+796delinsAAAAAAAAAAAAAG
ENST00000652672.2:c.4933+783_4933+796delinsAAAAAAAAAAAAAG ENSP00000498906.2:n.4933+783_4933+796delinsAAAAAAAAAAAAAG
ENST00000484087.6:c.1636+783_1636+796delinsAAAAAAAAAAAAAG ENSP00000419481.2:n.1636+783_1636+796delinsAAAAAAAAAAAAAG
ENST00000357654.9:c.5074+783_5074+796delinsAAAAAAAAAAAAAG MANE Select ENSP00000350283.3:n.5074+783_5074+796delinsAAAAAAAAAAAAAG
ENST00000471181.7:c.5137+783_5137+796delinsAAAAAAAAAAAAAG ENSP00000418960.2:n.5137+783_5137+796delinsAAAAAAAAAAAAAG
ENST00000644379.1:c.1461+783_1461+796delinsAAAAAAAAAAAAAG
ENST00000352993.7:c.1648+783_1648+796delinsAAAAAAAAAAAAAG ENSP00000312236.5:n.1648+783_1648+796delinsAAAAAAAAAAAAAG
ENST00000357654.7:c.5074+783_5074+796delinsAAAAAAAAAAAAAG ENSP00000350283.3:n.5074+783_5074+796delinsAAAAAAAAAAAAAG
ENST00000461221.5:c.*4857+783_*4857+796delinsAAAAAAAAAAAAAG ENSP00000418548.1:n.*4857+783_*4857+796delinsAAAAAAAAAAAAAG
ENST00000468300.5:c.1762+783_1762+796delinsAAAAAAAAAAAAAG ENSP00000417148.1:n.1762+783_1762+796delinsAAAAAAAAAAAAAG
ENST00000471181.6:c.5137+783_5137+796delinsAAAAAAAAAAAAAG ENSP00000418960.2:n.5137+783_5137+796delinsAAAAAAAAAAAAAG
ENST00000478531.5:c.1762+783_1762+796delinsAAAAAAAAAAAAAG ENSP00000420412.1:n.1762+783_1762+796delinsAAAAAAAAAAAAAG
ENST00000484087.5:c.1387+783_1387+796delinsAAAAAAAAAAAAAG ENSP00000419481.1:n.1387+783_1387+796delinsAAAAAAAAAAAAAG
ENST00000491747.6:c.1762+783_1762+796delinsAAAAAAAAAAAAAG ENSP00000420705.2:n.1762+783_1762+796delinsAAAAAAAAAAAAAG
ENST00000493795.5:c.4933+783_4933+796delinsAAAAAAAAAAAAAG ENSP00000418775.1:n.4933+783_4933+796delinsAAAAAAAAAAAAAG
ENST00000493919.5:c.1624+783_1624+796delinsAAAAAAAAAAAAAG ENSP00000418819.1:n.1624+783_1624+796delinsAAAAAAAAAAAAAG
ENST00000586385.5:c.5-2874_5-2861delinsAAAAAAAAAAAAAG ENSP00000465818.1:n.5-2874_5-2861delinsAAAAAAAAAAAAAG
ENST00000591534.5:c.547+783_547+796delinsAAAAAAAAAAAAAG ENSP00000467329.1:n.547+783_547+796delinsAAAAAAAAAAAAAG
ENST00000591849.5:c.-98-16635_-98-16622delinsAAAAAAAAAAAAAG ENSP00000465347.1:n.-98-16635_-98-16622delinsAAAAAAAAAAAAAG
NM_007294.3:c.5074+783_5074+796delinsAAAAAAAAAAAAAG , LRG_292t1:c.5074+783_5074+796delinsAAAAAAAAAAAAAG NP_009225.1:n.5074+783_5074+796delinsAAAAAAAAAAAAAG
NM_007297.3:c.4933+783_4933+796delinsAAAAAAAAAAAAAG NP_009228.2:n.4933+783_4933+796delinsAAAAAAAAAAAAAG
NM_007298.3:c.1762+783_1762+796delinsAAAAAAAAAAAAAG NP_009229.2:n.1762+783_1762+796delinsAAAAAAAAAAAAAG
NM_007299.3:c.1762+783_1762+796delinsAAAAAAAAAAAAAG NP_009230.2:n.1762+783_1762+796delinsAAAAAAAAAAAAAG
NM_007300.3:c.5137+783_5137+796delinsAAAAAAAAAAAAAG NP_009231.2:n.5137+783_5137+796delinsAAAAAAAAAAAAAG
NR_027676.1:n.5210+783_5210+796delinsAAAAAAAAAAAAAG
NM_007294.4:c.5074+783_5074+796delinsAAAAAAAAAAAAAG MANE Select NP_009225.1:n.5074+783_5074+796delinsAAAAAAAAAAAAAG
NM_007297.4:c.4933+783_4933+796delinsAAAAAAAAAAAAAG NP_009228.2:n.4933+783_4933+796delinsAAAAAAAAAAAAAG
NM_007299.4:c.1762+783_1762+796delinsAAAAAAAAAAAAAG NP_009230.2:n.1762+783_1762+796delinsAAAAAAAAAAAAAG
NM_007300.4:c.5137+783_5137+796delinsAAAAAAAAAAAAAG NP_009231.2:n.5137+783_5137+796delinsAAAAAAAAAAAAAG
NR_027676.2:n.5251+783_5251+796delinsAAAAAAAAAAAAAG