Canonical Allele Identifier: CA2809539287

Gene: BRCA1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43067416A>G , CM000679.2:g.43067416A>G	GRCh38
NC_000017.10:g.41219433A>G , CM000679.1:g.41219433A>G	GRCh37
NC_000017.9:g.38472959A>G	NCBI36
NG_005905.2:g.150568T>C , LRG_292:g.150568T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461574.2:c.5071+192T>C	ENSP00000417241.2:n.5071+192T>C
ENST00000470026.6:c.5074+192T>C	ENSP00000419274.2:n.5074+192T>C
ENST00000473961.6:c.4948+192T>C	ENSP00000420201.2:n.4948+192T>C
ENST00000476777.6:c.5068+192T>C	ENSP00000417554.2:n.5068+192T>C
ENST00000477152.6:c.4996+192T>C	ENSP00000419988.2:n.4996+192T>C
ENST00000478531.6:c.1762+192T>C	ENSP00000420412.2:n.1762+192T>C
ENST00000489037.2:c.4996+192T>C	ENSP00000420781.2:n.4996+192T>C
ENST00000493919.6:c.1624+192T>C	ENSP00000418819.2:n.1624+192T>C
ENST00000494123.6:c.5074+192T>C	ENSP00000419103.2:n.5074+192T>C
ENST00000497488.2:c.4186+192T>C	ENSP00000418986.2:n.4186+192T>C
ENST00000618469.2:c.5074+192T>C	ENSP00000478114.2:n.5074+192T>C
ENST00000634433.2:c.4951+192T>C	ENSP00000489431.2:n.4951+192T>C
ENST00000644379.2:c.5140+192T>C	ENSP00000496570.2:n.5140+192T>C
ENST00000644555.2:c.1624+192T>C	ENSP00000494614.2:n.1624+192T>C
ENST00000652672.2:c.4933+192T>C	ENSP00000498906.2:n.4933+192T>C
ENST00000484087.6:c.1636+192T>C	ENSP00000419481.2:n.1636+192T>C
ENST00000357654.9:c.5074+192T>C MANE Select	ENSP00000350283.3:n.5074+192T>C
ENST00000471181.7:c.5137+192T>C	ENSP00000418960.2:n.5137+192T>C
ENST00000644379.1:c.1461+192T>C
ENST00000352993.7:c.1648+192T>C	ENSP00000312236.5:n.1648+192T>C
ENST00000357654.7:c.5074+192T>C	ENSP00000350283.3:n.5074+192T>C
ENST00000461221.5:c.*4857+192T>C	ENSP00000418548.1:n.*4857+192T>C
ENST00000468300.5:c.1762+192T>C	ENSP00000417148.1:n.1762+192T>C
ENST00000471181.6:c.5137+192T>C	ENSP00000418960.2:n.5137+192T>C
ENST00000472490.1:n.419T>C
ENST00000478531.5:c.1762+192T>C	ENSP00000420412.1:n.1762+192T>C
ENST00000484087.5:c.1387+192T>C	ENSP00000419481.1:n.1387+192T>C
ENST00000491747.6:c.1762+192T>C	ENSP00000420705.2:n.1762+192T>C
ENST00000493795.5:c.4933+192T>C	ENSP00000418775.1:n.4933+192T>C
ENST00000493919.5:c.1624+192T>C	ENSP00000418819.1:n.1624+192T>C
ENST00000586385.5:c.5-3465T>C	ENSP00000465818.1:n.5-3465T>C
ENST00000591534.5:c.547+192T>C	ENSP00000467329.1:n.547+192T>C
ENST00000591849.5:c.-98-17226T>C	ENSP00000465347.1:n.-98-17226T>C
NM_007294.3:c.5074+192T>C , LRG_292t1:c.5074+192T>C	NP_009225.1:n.5074+192T>C
NM_007297.3:c.4933+192T>C	NP_009228.2:n.4933+192T>C
NM_007298.3:c.1762+192T>C	NP_009229.2:n.1762+192T>C
NM_007299.3:c.1762+192T>C	NP_009230.2:n.1762+192T>C
NM_007300.3:c.5137+192T>C	NP_009231.2:n.5137+192T>C
NR_027676.1:n.5210+192T>C
NM_007294.4:c.5074+192T>C MANE Select	NP_009225.1:n.5074+192T>C
NM_007297.4:c.4933+192T>C	NP_009228.2:n.4933+192T>C
NM_007299.4:c.1762+192T>C	NP_009230.2:n.1762+192T>C
NM_007300.4:c.5137+192T>C	NP_009231.2:n.5137+192T>C
NR_027676.2:n.5251+192T>C