Canonical Allele Identifier: CA2260775515

Gene: BRCA1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43076570_43076571delinsTC , CM000679.2:g.43076570_43076571delinsTC	GRCh38
NC_000017.10:g.41228587_41228588delinsTC , CM000679.1:g.41228587_41228588delinsTC	GRCh37
NC_000017.9:g.38482113_38482114delinsTC	NCBI36
NG_005905.2:g.141413_141414delinsGA , LRG_292:g.141413_141414delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461574.2:c.4398_4399delinsGA	ENSP00000417241.2:p.Gln1466=
ENST00000470026.6:c.4401_4402delinsGA	ENSP00000419274.2:p.Gln1467=
ENST00000473961.6:c.4275_4276delinsGA	ENSP00000420201.2:p.Gln1425=
ENST00000476777.6:c.4395_4396delinsGA	ENSP00000417554.2:p.Gln1465=
ENST00000477152.6:c.4323_4324delinsGA	ENSP00000419988.2:p.Gln1441=
ENST00000478531.6:c.1089_1090delinsGA	ENSP00000420412.2:p.Gln363=
ENST00000489037.2:c.4323_4324delinsGA	ENSP00000420781.2:p.Gln1441=
ENST00000493919.6:c.951_952delinsGA	ENSP00000418819.2:p.Gln317=
ENST00000494123.6:c.4401_4402delinsGA	ENSP00000419103.2:p.Gln1467=
ENST00000497488.2:c.3513_3514delinsGA	ENSP00000418986.2:p.Gln1171=
ENST00000618469.2:c.4401_4402delinsGA	ENSP00000478114.2:p.Gln1467=
ENST00000634433.2:c.4278_4279delinsGA	ENSP00000489431.2:p.Gln1426=
ENST00000644379.2:c.4467_4468delinsGA	ENSP00000496570.2:p.Gln1489=
ENST00000644555.2:c.951_952delinsGA	ENSP00000494614.2:p.Gln317=
ENST00000652672.2:c.4260_4261delinsGA	ENSP00000498906.2:p.Gln1420=
ENST00000484087.6:c.963_964delinsGA	ENSP00000419481.2:p.Gln321=
ENST00000700182.1:c.1008_1009delinsGA	ENSP00000514849.1:p.Gln336=
ENST00000357654.9:c.4401_4402delinsGA MANE Select	ENSP00000350283.3:p.Gln1467=
ENST00000471181.7:c.4464_4465delinsGA	ENSP00000418960.2:p.Gln1488=
ENST00000644379.1:c.788_789delinsGA
ENST00000352993.7:c.975_976delinsGA	ENSP00000312236.5:p.Gln325=
ENST00000357654.7:c.4401_4402delinsGA	ENSP00000350283.3:p.Gln1467=
ENST00000461221.5:c.*4184_*4185delinsGA	ENSP00000418548.1:n.*4184_*4185delinsGA
ENST00000461574.1:c.692_693delinsGA
ENST00000468300.5:c.1089_1090delinsGA	ENSP00000417148.1:p.Gln363=
ENST00000471181.6:c.4464_4465delinsGA	ENSP00000418960.2:p.Gln1488=
ENST00000478531.5:c.1089_1090delinsGA	ENSP00000420412.1:p.Gln363=
ENST00000484087.5:c.714_715delinsGA	ENSP00000419481.1:p.Gln238=
ENST00000487825.5:c.717_718delinsGA	ENSP00000418212.1:p.Gln239=
ENST00000491747.6:c.1089_1090delinsGA	ENSP00000420705.2:p.Gln363=
ENST00000493795.5:c.4260_4261delinsGA	ENSP00000418775.1:p.Gln1420=
ENST00000493919.5:c.951_952delinsGA	ENSP00000418819.1:p.Gln317=
ENST00000586385.5:c.5-12620_5-12619delinsGA	ENSP00000465818.1:n.5-12620_5-12619delinsGA
ENST00000591534.5:c.-43-2050_-43-2049delinsGA	ENSP00000467329.1:n.-43-2050_-43-2049delinsGA
ENST00000591849.5:c.-98-26381_-98-26380delinsGA	ENSP00000465347.1:n.-98-26381_-98-26380delinsGA
ENST00000621897.1:n.292_293delinsGA
NM_007294.3:c.4401_4402delinsGA , LRG_292t1:c.4401_4402delinsGA	NP_009225.1:p.Gln1467=
NM_007297.3:c.4260_4261delinsGA	NP_009228.2:p.Gln1420=
NM_007298.3:c.1089_1090delinsGA	NP_009229.2:p.Gln363=
NM_007299.3:c.1089_1090delinsGA	NP_009230.2:p.Gln363=
NM_007300.3:c.4464_4465delinsGA	NP_009231.2:p.Gln1488=
NR_027676.1:n.4537_4538delinsGA
NM_007294.4:c.4401_4402delinsGA MANE Select	NP_009225.1:p.Gln1467=
NM_007297.4:c.4260_4261delinsGA	NP_009228.2:p.Gln1420=
NM_007299.4:c.1089_1090delinsGA	NP_009230.2:p.Gln363=
NM_007300.4:c.4464_4465delinsGA	NP_009231.2:p.Gln1488=
NR_027676.2:n.4578_4579delinsGA