Canonical Allele Identifier: CA2260761908
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43047561_43047563delinsTAC , CM000679.2:g.43047561_43047563delinsTAC GRCh38
NC_000017.10:g.41199578_41199580delinsTAC , CM000679.1:g.41199578_41199580delinsTAC GRCh37
NC_000017.9:g.38453104_38453106delinsTAC NCBI36
NG_005905.2:g.170421_170423delinsGTA , LRG_292:g.170421_170423delinsGTA

Transcript Alleles

HGVS Amino-acid change
ENST00000461574.2:c.5464+80_5464+82delinsGTA ENSP00000417241.2:n.5464+80_5464+82delins...
ENST00000470026.6:c.5467+80_5467+82delinsGTA ENSP00000419274.2:n.5467+80_5467+82delins...
ENST00000473961.6:c.5341+80_5341+82delinsGTA ENSP00000420201.2:n.5341+80_5341+82delins...
ENST00000476777.6:c.5461+80_5461+82delinsGTA ENSP00000417554.2:n.5461+80_5461+82delins...
ENST00000477152.6:c.5389+80_5389+82delinsGTA ENSP00000419988.2:n.5389+80_5389+82delins...
ENST00000478531.6:c.2155+80_2155+82delinsGTA ENSP00000420412.2:n.2155+80_2155+82delins...
ENST00000489037.2:c.5389+80_5389+82delinsGTA ENSP00000420781.2:n.5389+80_5389+82delins...
ENST00000493919.6:c.2017+80_2017+82delinsGTA ENSP00000418819.2:n.2017+80_2017+82delins...
ENST00000494123.6:c.5467+80_5467+82delinsGTA ENSP00000419103.2:n.5467+80_5467+82delins...
ENST00000497488.2:c.4579+80_4579+82delinsGTA ENSP00000418986.2:n.4579+80_4579+82delins...
ENST00000618469.2:c.5467+80_5467+82delinsGTA ENSP00000478114.2:n.5467+80_5467+82delins...
ENST00000634433.2:c.5344+80_5344+82delinsGTA ENSP00000489431.2:n.5344+80_5344+82delins...
ENST00000644379.2:c.5533+80_5533+82delinsGTA ENSP00000496570.2:n.5533+80_5533+82delins...
ENST00000644555.2:c.2017+80_2017+82delinsGTA ENSP00000494614.2:n.2017+80_2017+82delins...
ENST00000652672.2:c.5326+80_5326+82delinsGTA ENSP00000498906.2:n.5326+80_5326+82delins...
ENST00000484087.6:c.2029+80_2029+82delinsGTA ENSP00000419481.2:n.2029+80_2029+82delins...
ENST00000700081.1:n.1350+80_1350+82delinsGTA
ENST00000700082.1:n.831+80_831+82delinsGTA
ENST00000357654.9:c.5467+80_5467+82delinsGTA MANE Select ENSP00000350283.3:n.5467+80_5467+82delins...
ENST00000471181.7:c.5530+80_5530+82delinsGTA ENSP00000418960.2:n.5530+80_5530+82delins...
ENST00000644379.1:c.1854+80_1854+82delinsGTA
ENST00000352993.7:c.2041+80_2041+82delinsGTA ENSP00000312236.5:n.2041+80_2041+82delins...
ENST00000357654.7:c.5467+80_5467+82delinsGTA ENSP00000350283.3:n.5467+80_5467+82delins...
ENST00000461221.5:c.*5250+80_*5250+82delinsGTA ENSP00000418548.1:n.*5250+80_*5250+82deli...
ENST00000468300.5:c.2081+80_2081+82delinsGTA ENSP00000417148.1:n.2081+80_2081+82delins...
ENST00000471181.6:c.5530+80_5530+82delinsGTA ENSP00000418960.2:n.5530+80_5530+82delins...
ENST00000491747.6:c.2155+80_2155+82delinsGTA ENSP00000420705.2:n.2155+80_2155+82delins...
ENST00000493795.5:c.5326+80_5326+82delinsGTA ENSP00000418775.1:n.5326+80_5326+82delins...
ENST00000586385.5:c.397+80_397+82delinsGTA ENSP00000465818.1:n.397+80_397+82delinsGT...
ENST00000591534.5:c.940+80_940+82delinsGTA ENSP00000467329.1:n.940+80_940+82delinsGT...
ENST00000591849.5:c.166+80_166+82delinsGTA ENSP00000465347.1:n.166+80_166+82delinsGT...
NM_007294.3:c.5467+80_5467+82delinsGTA , LRG_292t1:c.5467+80_5467+82delinsGTA NP_009225.1:n.5467+80_5467+82delinsGTA
NM_007297.3:c.5326+80_5326+82delinsGTA NP_009228.2:n.5326+80_5326+82delinsGTA
NM_007298.3:c.2155+80_2155+82delinsGTA NP_009229.2:n.2155+80_2155+82delinsGTA
NM_007299.3:c.2081+80_2081+82delinsGTA NP_009230.2:n.2081+80_2081+82delinsGTA
NM_007300.3:c.5530+80_5530+82delinsGTA NP_009231.2:n.5530+80_5530+82delinsGTA
NR_027676.1:n.5603+80_5603+82delinsGTA
NM_007294.4:c.5467+80_5467+82delinsGTA MANE Select NP_009225.1:n.5467+80_5467+82delinsGTA
NM_007297.4:c.5326+80_5326+82delinsGTA NP_009228.2:n.5326+80_5326+82delinsGTA
NM_007299.4:c.2081+80_2081+82delinsGTA NP_009230.2:n.2081+80_2081+82delinsGTA
NM_007300.4:c.5530+80_5530+82delinsGTA NP_009231.2:n.5530+80_5530+82delinsGTA
NR_027676.2:n.5644+80_5644+82delinsGTA