Canonical Allele Identifier: CA003033

Gene: BRCA1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43071102T>C , CM000679.2:g.43071102T>C	GRCh38
NC_000017.10:g.41223119T>C , CM000679.1:g.41223119T>C	GRCh37
NC_000017.9:g.38476645T>C	NCBI36
NG_005905.2:g.146882A>G , LRG_292:g.146882A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461574.2:c.4809A>G	ENSP00000417241.2:p.Gln1603=
ENST00000470026.6:c.4812A>G	ENSP00000419274.2:p.Gln1604=
ENST00000473961.6:c.4686A>G	ENSP00000420201.2:p.Gln1562=
ENST00000476777.6:c.4806A>G	ENSP00000417554.2:p.Gln1602=
ENST00000477152.6:c.4734A>G	ENSP00000419988.2:p.Gln1578=
ENST00000478531.6:c.1500A>G	ENSP00000420412.2:p.Gln500=
ENST00000489037.2:c.4734A>G	ENSP00000420781.2:p.Gln1578=
ENST00000493919.6:c.1362A>G	ENSP00000418819.2:p.Gln454=
ENST00000494123.6:c.4812A>G	ENSP00000419103.2:p.Gln1604=
ENST00000497488.2:c.3924A>G	ENSP00000418986.2:p.Gln1308=
ENST00000618469.2:c.4812A>G	ENSP00000478114.2:p.Gln1604=
ENST00000634433.2:c.4689A>G	ENSP00000489431.2:p.Gln1563=
ENST00000644379.2:c.4878A>G	ENSP00000496570.2:p.Gln1626=
ENST00000644555.2:c.1362A>G	ENSP00000494614.2:p.Gln454=
ENST00000652672.2:c.4671A>G	ENSP00000498906.2:p.Gln1557=
ENST00000484087.6:c.1374A>G	ENSP00000419481.2:p.Gln458=
ENST00000700182.1:c.1419A>G	ENSP00000514849.1:p.Gln473=
ENST00000357654.9:c.4812A>G MANE Select	ENSP00000350283.3:p.Gln1604=
ENST00000471181.7:c.4875A>G	ENSP00000418960.2:p.Gln1625=
ENST00000644379.1:c.1199A>G
ENST00000352993.7:c.1386A>G	ENSP00000312236.5:p.Gln462=
ENST00000357654.7:c.4812A>G	ENSP00000350283.3:p.Gln1604=
ENST00000461221.5:c.*4595A>G	ENSP00000418548.1:n.*4595A>G
ENST00000468300.5:c.1500A>G	ENSP00000417148.1:p.Gln500=
ENST00000471181.6:c.4875A>G	ENSP00000418960.2:p.Gln1625=
ENST00000478531.5:c.1500A>G	ENSP00000420412.1:p.Gln500=
ENST00000484087.5:c.1125A>G	ENSP00000419481.1:p.Gln375=
ENST00000491747.6:c.1500A>G	ENSP00000420705.2:p.Gln500=
ENST00000493795.5:c.4671A>G	ENSP00000418775.1:p.Gln1557=
ENST00000493919.5:c.1362A>G	ENSP00000418819.1:p.Gln454=
ENST00000586385.5:c.5-7151A>G	ENSP00000465818.1:n.5-7151A>G
ENST00000591534.5:c.285A>G	ENSP00000467329.1:p.Gln95=
ENST00000591849.5:c.-98-20912A>G	ENSP00000465347.1:n.-98-20912A>G
NM_007294.3:c.4812A>G , LRG_292t1:c.4812A>G	NP_009225.1:p.Gln1604=
NM_007297.3:c.4671A>G	NP_009228.2:p.Gln1557=
NM_007298.3:c.1500A>G	NP_009229.2:p.Gln500=
NM_007299.3:c.1500A>G	NP_009230.2:p.Gln500=
NM_007300.3:c.4875A>G	NP_009231.2:p.Gln1625=
NR_027676.1:n.4948A>G
NM_007294.4:c.4812A>G MANE Select	NP_009225.1:p.Gln1604=
NM_007297.4:c.4671A>G	NP_009228.2:p.Gln1557=
NM_007299.4:c.1500A>G	NP_009230.2:p.Gln500=
NM_007300.4:c.4875A>G	NP_009231.2:p.Gln1625=
NR_027676.2:n.4989A>G