Canonical Allele Identifier: CA10592679

Gene: BRCA1

Linked Data

• dbSNP Id: rs2052729085
• MyVariant Identifiers: chr17:g.41228560A>T (hg19) ; chr17:g.43076543A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43076543A>T , CM000679.2:g.43076543A>T	GRCh38
NC_000017.10:g.41228560A>T , CM000679.1:g.41228560A>T	GRCh37
NC_000017.9:g.38482086A>T	NCBI36
NG_005905.2:g.141441T>A , LRG_292:g.141441T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461574.2:c.4426T>A	ENSP00000417241.2:p.Phe1476Ile
ENST00000470026.6:c.4429T>A	ENSP00000419274.2:p.Phe1477Ile
ENST00000473961.6:c.4303T>A	ENSP00000420201.2:p.Phe1435Ile
ENST00000476777.6:c.4423T>A	ENSP00000417554.2:p.Phe1475Ile
ENST00000477152.6:c.4351T>A	ENSP00000419988.2:p.Phe1451Ile
ENST00000478531.6:c.1117T>A	ENSP00000420412.2:p.Phe373Ile
ENST00000489037.2:c.4351T>A	ENSP00000420781.2:p.Phe1451Ile
ENST00000493919.6:c.979T>A	ENSP00000418819.2:p.Phe327Ile
ENST00000494123.6:c.4429T>A	ENSP00000419103.2:p.Phe1477Ile
ENST00000497488.2:c.3541T>A	ENSP00000418986.2:p.Phe1181Ile
ENST00000618469.2:c.4429T>A	ENSP00000478114.2:p.Phe1477Ile
ENST00000634433.2:c.4306T>A	ENSP00000489431.2:p.Phe1436Ile
ENST00000644379.2:c.4495T>A	ENSP00000496570.2:p.Phe1499Ile
ENST00000644555.2:c.979T>A	ENSP00000494614.2:p.Phe327Ile
ENST00000652672.2:c.4288T>A	ENSP00000498906.2:p.Phe1430Ile
ENST00000484087.6:c.991T>A	ENSP00000419481.2:p.Phe331Ile
ENST00000700182.1:c.1036T>A	ENSP00000514849.1:p.Phe346Ile
ENST00000357654.9:c.4429T>A MANE Select	ENSP00000350283.3:p.Phe1477Ile
ENST00000471181.7:c.4492T>A	ENSP00000418960.2:p.Phe1498Ile
ENST00000644379.1:c.816T>A
ENST00000352993.7:c.1003T>A	ENSP00000312236.5:p.Phe335Ile
ENST00000357654.7:c.4429T>A	ENSP00000350283.3:p.Phe1477Ile
ENST00000461221.5:c.*4212T>A	ENSP00000418548.1:n.*4212T>A
ENST00000461574.1:c.720T>A
ENST00000468300.5:c.1117T>A	ENSP00000417148.1:p.Phe373Ile
ENST00000471181.6:c.4492T>A	ENSP00000418960.2:p.Phe1498Ile
ENST00000478531.5:c.1117T>A	ENSP00000420412.1:p.Phe373Ile
ENST00000484087.5:c.742T>A	ENSP00000419481.1:p.Phe248Ile
ENST00000487825.5:c.745T>A	ENSP00000418212.1:p.Phe249Ile
ENST00000491747.6:c.1117T>A	ENSP00000420705.2:p.Phe373Ile
ENST00000493795.5:c.4288T>A	ENSP00000418775.1:p.Phe1430Ile
ENST00000493919.5:c.979T>A	ENSP00000418819.1:p.Phe327Ile
ENST00000586385.5:c.5-12592T>A	ENSP00000465818.1:n.5-12592T>A
ENST00000591534.5:c.-43-2022T>A	ENSP00000467329.1:n.-43-2022T>A
ENST00000591849.5:c.-98-26353T>A	ENSP00000465347.1:n.-98-26353T>A
ENST00000621897.1:n.320T>A
NM_007294.3:c.4429T>A , LRG_292t1:c.4429T>A	NP_009225.1:p.Phe1477Ile
NM_007297.3:c.4288T>A	NP_009228.2:p.Phe1430Ile
NM_007298.3:c.1117T>A	NP_009229.2:p.Phe373Ile
NM_007299.3:c.1117T>A	NP_009230.2:p.Phe373Ile
NM_007300.3:c.4492T>A	NP_009231.2:p.Phe1498Ile
NR_027676.1:n.4565T>A
NM_007294.4:c.4429T>A MANE Select	NP_009225.1:p.Phe1477Ile
NM_007297.4:c.4288T>A	NP_009228.2:p.Phe1430Ile
NM_007299.4:c.1117T>A	NP_009230.2:p.Phe373Ile
NM_007300.4:c.4492T>A	NP_009231.2:p.Phe1498Ile
NR_027676.2:n.4606T>A