Canonical Allele Identifier: CA10591068

Gene: BRCA1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43057093G>A , CM000679.2:g.43057093G>A	GRCh38
NC_000017.10:g.41209110G>A , CM000679.1:g.41209110G>A	GRCh37
NC_000017.9:g.38462636G>A	NCBI36
NG_005905.2:g.160891C>T , LRG_292:g.160891C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_007294.4:c.5236C>T MANE Select	NP_009225.1:p.His1746Tyr
ENST00000357654.9:c.5236C>T MANE Select	ENSP00000350283.3:p.His1746Tyr
NM_007294.3:c.5236C>T , LRG_292t1:c.5236C>T	NP_009225.1:p.His1746Tyr
NM_007297.3:c.5095C>T	NP_009228.2:p.His1699Tyr
NM_007297.4:c.5095C>T	NP_009228.2:p.His1699Tyr
NM_007298.3:c.1924C>T	NP_009229.2:p.His642Tyr
NM_007299.3:c.1924C>T	NP_009230.2:p.His642Tyr
NM_007299.4:c.1924C>T	NP_009230.2:p.His642Tyr
NM_007300.3:c.5299C>T	NP_009231.2:p.His1767Tyr
NM_007300.4:c.5299C>T	NP_009231.2:p.His1767Tyr
NR_027676.1:n.5372C>T
NR_027676.2:n.5413C>T
ENST00000352993.7:c.1810C>T	ENSP00000312236.5:p.His604Tyr
ENST00000357654.7:c.5236C>T	ENSP00000350283.3:p.His1746Tyr
ENST00000461221.5:c.*5019C>T	ENSP00000418548.1:n.*5019C>T
ENST00000461574.2:c.5233C>T	ENSP00000417241.2:p.His1745Tyr
ENST00000468300.5:c.1924C>T	ENSP00000417148.1:p.His642Tyr
ENST00000470026.6:c.5236C>T	ENSP00000419274.2:p.His1746Tyr
ENST00000471181.6:c.5299C>T	ENSP00000418960.2:p.His1767Tyr
ENST00000471181.7:c.5299C>T	ENSP00000418960.2:p.His1767Tyr
ENST00000473961.6:c.5110C>T	ENSP00000420201.2:p.His1704Tyr
ENST00000476777.6:c.5230C>T	ENSP00000417554.2:p.His1744Tyr
ENST00000477152.6:c.5158C>T	ENSP00000419988.2:p.His1720Tyr
ENST00000478531.6:c.1924C>T	ENSP00000420412.2:p.His642Tyr
ENST00000484087.6:c.1798C>T	ENSP00000419481.2:p.His600Tyr
ENST00000489037.2:c.5158C>T	ENSP00000420781.2:p.His1720Tyr
ENST00000491747.6:c.1924C>T	ENSP00000420705.2:p.His642Tyr
ENST00000493795.5:c.5095C>T	ENSP00000418775.1:p.His1699Tyr
ENST00000493919.6:c.1786C>T	ENSP00000418819.2:p.His596Tyr
ENST00000494123.6:c.5236C>T	ENSP00000419103.2:p.His1746Tyr
ENST00000497488.2:c.4348C>T	ENSP00000418986.2:p.His1450Tyr
ENST00000586385.5:c.166C>T	ENSP00000465818.1:p.His56Tyr
ENST00000591534.5:c.709C>T	ENSP00000467329.1:p.His237Tyr
ENST00000591849.5:c.-98-6903C>T	ENSP00000465347.1:n.-98-6903C>T
ENST00000618469.2:c.5236C>T	ENSP00000478114.2:p.His1746Tyr
ENST00000634433.2:c.5113C>T	ENSP00000489431.2:p.His1705Tyr
ENST00000644379.1:c.1623C>T
ENST00000644379.2:c.5302C>T	ENSP00000496570.2:p.His1768Tyr
ENST00000644555.2:c.1786C>T	ENSP00000494614.2:p.His596Tyr
ENST00000652672.2:c.5095C>T	ENSP00000498906.2:p.His1699Tyr