Canonical Allele Identifier: CA2260775456

Gene: BRCA1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43076507T= , CM000679.2:g.43076507T=	GRCh38
NC_000017.10:g.41228524T= , CM000679.1:g.41228524T=	GRCh37
NC_000017.9:g.38482050T=	NCBI36
NG_005905.2:g.141477A= , LRG_292:g.141477A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000461574.2:c.4462A=	ENSP00000417241.2:p.Lys1488=
ENST00000470026.6:c.4465A=	ENSP00000419274.2:p.Lys1489=
ENST00000473961.6:c.4339A=	ENSP00000420201.2:p.Lys1447=
ENST00000476777.6:c.4459A=	ENSP00000417554.2:p.Lys1487=
ENST00000477152.6:c.4387A=	ENSP00000419988.2:p.Lys1463=
ENST00000478531.6:c.1153A=	ENSP00000420412.2:p.Lys385=
ENST00000489037.2:c.4387A=	ENSP00000420781.2:p.Lys1463=
ENST00000493919.6:c.1015A=	ENSP00000418819.2:p.Lys339=
ENST00000494123.6:c.4465A=	ENSP00000419103.2:p.Lys1489=
ENST00000497488.2:c.3577A=	ENSP00000418986.2:p.Lys1193=
ENST00000618469.2:c.4465A=	ENSP00000478114.2:p.Lys1489=
ENST00000634433.2:c.4342A=	ENSP00000489431.2:p.Lys1448=
ENST00000644379.2:c.4531A=	ENSP00000496570.2:p.Lys1511=
ENST00000644555.2:c.1015A=	ENSP00000494614.2:p.Lys339=
ENST00000652672.2:c.4324A=	ENSP00000498906.2:p.Lys1442=
ENST00000484087.6:c.1027A=	ENSP00000419481.2:p.Lys343=
ENST00000700182.1:c.1072A=	ENSP00000514849.1:p.Lys358=
ENST00000357654.9:c.4465A= MANE Select	ENSP00000350283.3:p.Lys1489=
ENST00000471181.7:c.4528A=	ENSP00000418960.2:p.Lys1510=
ENST00000644379.1:c.852A=
ENST00000352993.7:c.1039A=	ENSP00000312236.5:p.Lys347=
ENST00000357654.7:c.4465A=	ENSP00000350283.3:p.Lys1489=
ENST00000461221.5:c.*4248A=	ENSP00000418548.1:n.*4248A=
ENST00000468300.5:c.1153A=	ENSP00000417148.1:p.Lys385=
ENST00000471181.6:c.4528A=	ENSP00000418960.2:p.Lys1510=
ENST00000478531.5:c.1153A=	ENSP00000420412.1:p.Lys385=
ENST00000484087.5:c.778A=	ENSP00000419481.1:p.Lys260=
ENST00000487825.5:c.781A=	ENSP00000418212.1:p.Lys261=
ENST00000491747.6:c.1153A=	ENSP00000420705.2:p.Lys385=
ENST00000493795.5:c.4324A=	ENSP00000418775.1:p.Lys1442=
ENST00000493919.5:c.1015A=	ENSP00000418819.1:p.Lys339=
ENST00000586385.5:c.5-12556A=	ENSP00000465818.1:n.5-12556A=
ENST00000591534.5:c.-43-1986A=	ENSP00000467329.1:n.-43-1986A=
ENST00000591849.5:c.-98-26317A=	ENSP00000465347.1:n.-98-26317A=
ENST00000621897.1:n.356A=
NM_007294.3:c.4465A= , LRG_292t1:c.4465A=	NP_009225.1:p.Lys1489=
NM_007297.3:c.4324A=	NP_009228.2:p.Lys1442=
NM_007298.3:c.1153A=	NP_009229.2:p.Lys385=
NM_007299.3:c.1153A=	NP_009230.2:p.Lys385=
NM_007300.3:c.4528A=	NP_009231.2:p.Lys1510=
NR_027676.1:n.4601A=
NM_007294.4:c.4465A= MANE Select	NP_009225.1:p.Lys1489=
NM_007297.4:c.4324A=	NP_009228.2:p.Lys1442=
NM_007299.4:c.1153A=	NP_009230.2:p.Lys385=
NM_007300.4:c.4528A=	NP_009231.2:p.Lys1510=
NR_027676.2:n.4642A=