Canonical Allele Identifier: CA2260761845

Gene: BRCA1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43047428_43047430delinsCAT , CM000679.2:g.43047428_43047430delinsCAT	GRCh38
NC_000017.10:g.41199445_41199447delinsCAT , CM000679.1:g.41199445_41199447delinsCAT	GRCh37
NC_000017.9:g.38452971_38452973delinsCAT	NCBI36
NG_005905.2:g.170554_170556delinsATG , LRG_292:g.170554_170556delinsATG

Transcript Alleles

HGVS	Amino-acid change
ENST00000461574.2:c.5464+213_5464+215delinsATG	ENSP00000417241.2:n.5464+213_5464+215deli...
ENST00000470026.6:c.5467+213_5467+215delinsATG	ENSP00000419274.2:n.5467+213_5467+215deli...
ENST00000473961.6:c.5341+213_5341+215delinsATG	ENSP00000420201.2:n.5341+213_5341+215deli...
ENST00000476777.6:c.5461+213_5461+215delinsATG	ENSP00000417554.2:n.5461+213_5461+215deli...
ENST00000477152.6:c.5389+213_5389+215delinsATG	ENSP00000419988.2:n.5389+213_5389+215deli...
ENST00000478531.6:c.2155+213_2155+215delinsATG	ENSP00000420412.2:n.2155+213_2155+215deli...
ENST00000489037.2:c.5389+213_5389+215delinsATG	ENSP00000420781.2:n.5389+213_5389+215deli...
ENST00000493919.6:c.2017+213_2017+215delinsATG	ENSP00000418819.2:n.2017+213_2017+215deli...
ENST00000494123.6:c.5467+213_5467+215delinsATG	ENSP00000419103.2:n.5467+213_5467+215deli...
ENST00000497488.2:c.4579+213_4579+215delinsATG	ENSP00000418986.2:n.4579+213_4579+215deli...
ENST00000618469.2:c.5467+213_5467+215delinsATG	ENSP00000478114.2:n.5467+213_5467+215deli...
ENST00000634433.2:c.5344+213_5344+215delinsATG	ENSP00000489431.2:n.5344+213_5344+215deli...
ENST00000644379.2:c.5533+213_5533+215delinsATG	ENSP00000496570.2:n.5533+213_5533+215deli...
ENST00000644555.2:c.2017+213_2017+215delinsATG	ENSP00000494614.2:n.2017+213_2017+215deli...
ENST00000652672.2:c.5326+213_5326+215delinsATG	ENSP00000498906.2:n.5326+213_5326+215deli...
ENST00000484087.6:c.2029+213_2029+215delinsATG	ENSP00000419481.2:n.2029+213_2029+215deli...
ENST00000700081.1:n.1350+213_1350+215delinsATG
ENST00000700082.1:n.831+213_831+215delinsATG
ENST00000357654.9:c.5467+213_5467+215delinsATG MANE Select	ENSP00000350283.3:n.5467+213_5467+215deli...
ENST00000471181.7:c.5530+213_5530+215delinsATG	ENSP00000418960.2:n.5530+213_5530+215deli...
ENST00000644379.1:c.1854+213_1854+215delinsATG
ENST00000352993.7:c.2041+213_2041+215delinsATG	ENSP00000312236.5:n.2041+213_2041+215deli...
ENST00000357654.7:c.5467+213_5467+215delinsATG	ENSP00000350283.3:n.5467+213_5467+215deli...
ENST00000461221.5:c.*5250+213_*5250+215delinsATG	ENSP00000418548.1:n.*5250+213_*5250+215de...
ENST00000468300.5:c.2081+213_2081+215delinsATG	ENSP00000417148.1:n.2081+213_2081+215deli...
ENST00000471181.6:c.5530+213_5530+215delinsATG	ENSP00000418960.2:n.5530+213_5530+215deli...
ENST00000491747.6:c.2155+213_2155+215delinsATG	ENSP00000420705.2:n.2155+213_2155+215deli...
ENST00000493795.5:c.5326+213_5326+215delinsATG	ENSP00000418775.1:n.5326+213_5326+215deli...
ENST00000586385.5:c.397+213_397+215delinsATG	ENSP00000465818.1:n.397+213_397+215delins...
ENST00000591534.5:c.940+213_940+215delinsATG	ENSP00000467329.1:n.940+213_940+215delins...
ENST00000591849.5:c.166+213_166+215delinsATG	ENSP00000465347.1:n.166+213_166+215delins...
NM_007294.3:c.5467+213_5467+215delinsATG , LRG_292t1:c.5467+213_5467+215delinsATG	NP_009225.1:n.5467+213_5467+215delinsATG
NM_007297.3:c.5326+213_5326+215delinsATG	NP_009228.2:n.5326+213_5326+215delinsATG
NM_007298.3:c.2155+213_2155+215delinsATG	NP_009229.2:n.2155+213_2155+215delinsATG
NM_007299.3:c.2081+213_2081+215delinsATG	NP_009230.2:n.2081+213_2081+215delinsATG
NM_007300.3:c.5530+213_5530+215delinsATG	NP_009231.2:n.5530+213_5530+215delinsATG
NR_027676.1:n.5603+213_5603+215delinsATG
NM_007294.4:c.5467+213_5467+215delinsATG MANE Select	NP_009225.1:n.5467+213_5467+215delinsATG
NM_007297.4:c.5326+213_5326+215delinsATG	NP_009228.2:n.5326+213_5326+215delinsATG
NM_007299.4:c.2081+213_2081+215delinsATG	NP_009230.2:n.2081+213_2081+215delinsATG
NM_007300.4:c.5530+213_5530+215delinsATG	NP_009231.2:n.5530+213_5530+215delinsATG
NR_027676.2:n.5644+213_5644+215delinsATG