Canonical Allele Identifier: CA2260770784
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43066668_43066670delinsCAA , CM000679.2:g.43066668_43066670delinsCAA GRCh38
NC_000017.10:g.41218685_41218687delinsCAA , CM000679.1:g.41218685_41218687delinsCAA GRCh37
NC_000017.9:g.38472211_38472213delinsCAA NCBI36
NG_005905.2:g.151314_151316delinsTTG , LRG_292:g.151314_151316delinsTTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000461574.2:c.5071+938_5071+940delinsTTG ENSP00000417241.2:n.5071+938_5071+940delinsTTG
ENST00000470026.6:c.5074+938_5074+940delinsTTG ENSP00000419274.2:n.5074+938_5074+940delinsTTG
ENST00000473961.6:c.4948+938_4948+940delinsTTG ENSP00000420201.2:n.4948+938_4948+940delinsTTG
ENST00000476777.6:c.5068+938_5068+940delinsTTG ENSP00000417554.2:n.5068+938_5068+940delinsTTG
ENST00000477152.6:c.4996+938_4996+940delinsTTG ENSP00000419988.2:n.4996+938_4996+940delinsTTG
ENST00000478531.6:c.1762+938_1762+940delinsTTG ENSP00000420412.2:n.1762+938_1762+940delinsTTG
ENST00000489037.2:c.4996+938_4996+940delinsTTG ENSP00000420781.2:n.4996+938_4996+940delinsTTG
ENST00000493919.6:c.1624+938_1624+940delinsTTG ENSP00000418819.2:n.1624+938_1624+940delinsTTG
ENST00000494123.6:c.5074+938_5074+940delinsTTG ENSP00000419103.2:n.5074+938_5074+940delinsTTG
ENST00000497488.2:c.4186+938_4186+940delinsTTG ENSP00000418986.2:n.4186+938_4186+940delinsTTG
ENST00000618469.2:c.5074+938_5074+940delinsTTG ENSP00000478114.2:n.5074+938_5074+940delinsTTG
ENST00000634433.2:c.4951+938_4951+940delinsTTG ENSP00000489431.2:n.4951+938_4951+940delinsTTG
ENST00000644379.2:c.5140+938_5140+940delinsTTG ENSP00000496570.2:n.5140+938_5140+940delinsTTG
ENST00000644555.2:c.1624+938_1624+940delinsTTG ENSP00000494614.2:n.1624+938_1624+940delinsTTG
ENST00000652672.2:c.4933+938_4933+940delinsTTG ENSP00000498906.2:n.4933+938_4933+940delinsTTG
ENST00000484087.6:c.1636+938_1636+940delinsTTG ENSP00000419481.2:n.1636+938_1636+940delinsTTG
ENST00000357654.9:c.5074+938_5074+940delinsTTG MANE Select ENSP00000350283.3:n.5074+938_5074+940delinsTTG
ENST00000471181.7:c.5137+938_5137+940delinsTTG ENSP00000418960.2:n.5137+938_5137+940delinsTTG
ENST00000644379.1:c.1461+938_1461+940delinsTTG
ENST00000352993.7:c.1648+938_1648+940delinsTTG ENSP00000312236.5:n.1648+938_1648+940delinsTTG
ENST00000357654.7:c.5074+938_5074+940delinsTTG ENSP00000350283.3:n.5074+938_5074+940delinsTTG
ENST00000461221.5:c.*4857+938_*4857+940delinsTTG ENSP00000418548.1:n.*4857+938_*4857+940delinsTTG
ENST00000468300.5:c.1762+938_1762+940delinsTTG ENSP00000417148.1:n.1762+938_1762+940delinsTTG
ENST00000471181.6:c.5137+938_5137+940delinsTTG ENSP00000418960.2:n.5137+938_5137+940delinsTTG
ENST00000478531.5:c.1762+938_1762+940delinsTTG ENSP00000420412.1:n.1762+938_1762+940delinsTTG
ENST00000484087.5:c.1387+938_1387+940delinsTTG ENSP00000419481.1:n.1387+938_1387+940delinsTTG
ENST00000491747.6:c.1762+938_1762+940delinsTTG ENSP00000420705.2:n.1762+938_1762+940delinsTTG
ENST00000493795.5:c.4933+938_4933+940delinsTTG ENSP00000418775.1:n.4933+938_4933+940delinsTTG
ENST00000493919.5:c.1624+938_1624+940delinsTTG ENSP00000418819.1:n.1624+938_1624+940delinsTTG
ENST00000586385.5:c.5-2719_5-2717delinsTTG ENSP00000465818.1:n.5-2719_5-2717delinsTTG
ENST00000591534.5:c.547+938_547+940delinsTTG ENSP00000467329.1:n.547+938_547+940delinsTTG
ENST00000591849.5:c.-98-16480_-98-16478delinsTTG ENSP00000465347.1:n.-98-16480_-98-16478delinsTTG
NM_007294.3:c.5074+938_5074+940delinsTTG , LRG_292t1:c.5074+938_5074+940delinsTTG NP_009225.1:n.5074+938_5074+940delinsTTG
NM_007297.3:c.4933+938_4933+940delinsTTG NP_009228.2:n.4933+938_4933+940delinsTTG
NM_007298.3:c.1762+938_1762+940delinsTTG NP_009229.2:n.1762+938_1762+940delinsTTG
NM_007299.3:c.1762+938_1762+940delinsTTG NP_009230.2:n.1762+938_1762+940delinsTTG
NM_007300.3:c.5137+938_5137+940delinsTTG NP_009231.2:n.5137+938_5137+940delinsTTG
NR_027676.1:n.5210+938_5210+940delinsTTG
NM_007294.4:c.5074+938_5074+940delinsTTG MANE Select NP_009225.1:n.5074+938_5074+940delinsTTG
NM_007297.4:c.4933+938_4933+940delinsTTG NP_009228.2:n.4933+938_4933+940delinsTTG
NM_007299.4:c.1762+938_1762+940delinsTTG NP_009230.2:n.1762+938_1762+940delinsTTG
NM_007300.4:c.5137+938_5137+940delinsTTG NP_009231.2:n.5137+938_5137+940delinsTTG
NR_027676.2:n.5251+938_5251+940delinsTTG