Canonical Allele Identifier: CA10591377

Gene: BRCA1

Linked Data

• ClinVar Variation Id: 868985
• ClinVar RCV Id: RCV001077997
• dbSNP Id: rs397509219
• MyVariant Identifiers: chr17:g.41219628T>A (hg19) ; chr17:g.43067611T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43067611T>A , CM000679.2:g.43067611T>A	GRCh38
NC_000017.10:g.41219628T>A , CM000679.1:g.41219628T>A	GRCh37
NC_000017.9:g.38473154T>A	NCBI36
NG_005905.2:g.150373A>T , LRG_292:g.150373A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000461574.2:c.5068A>T	ENSP00000417241.2:p.Thr1690Ser
ENST00000470026.6:c.5071A>T	ENSP00000419274.2:p.Thr1691Ser
ENST00000473961.6:c.4945A>T	ENSP00000420201.2:p.Thr1649Ser
ENST00000476777.6:c.5065A>T	ENSP00000417554.2:p.Thr1689Ser
ENST00000477152.6:c.4993A>T	ENSP00000419988.2:p.Thr1665Ser
ENST00000478531.6:c.1759A>T	ENSP00000420412.2:p.Thr587Ser
ENST00000489037.2:c.4993A>T	ENSP00000420781.2:p.Thr1665Ser
ENST00000493919.6:c.1621A>T	ENSP00000418819.2:p.Thr541Ser
ENST00000494123.6:c.5071A>T	ENSP00000419103.2:p.Thr1691Ser
ENST00000497488.2:c.4183A>T	ENSP00000418986.2:p.Thr1395Ser
ENST00000618469.2:c.5071A>T	ENSP00000478114.2:p.Thr1691Ser
ENST00000634433.2:c.4948A>T	ENSP00000489431.2:p.Thr1650Ser
ENST00000644379.2:c.5137A>T	ENSP00000496570.2:p.Thr1713Ser
ENST00000644555.2:c.1621A>T	ENSP00000494614.2:p.Thr541Ser
ENST00000652672.2:c.4930A>T	ENSP00000498906.2:p.Thr1644Ser
ENST00000484087.6:c.1633A>T	ENSP00000419481.2:p.Thr545Ser
ENST00000357654.9:c.5071A>T MANE Select	ENSP00000350283.3:p.Thr1691Ser
ENST00000471181.7:c.5134A>T	ENSP00000418960.2:p.Thr1712Ser
ENST00000644379.1:c.1458A>T
ENST00000352993.7:c.1645A>T	ENSP00000312236.5:p.Thr549Ser
ENST00000357654.7:c.5071A>T	ENSP00000350283.3:p.Thr1691Ser
ENST00000461221.5:c.*4854A>T	ENSP00000418548.1:n.*4854A>T
ENST00000468300.5:c.1759A>T	ENSP00000417148.1:p.Thr587Ser
ENST00000471181.6:c.5134A>T	ENSP00000418960.2:p.Thr1712Ser
ENST00000472490.1:n.224A>T
ENST00000478531.5:c.1759A>T	ENSP00000420412.1:p.Thr587Ser
ENST00000484087.5:c.1384A>T	ENSP00000419481.1:p.Thr462Ser
ENST00000491747.6:c.1759A>T	ENSP00000420705.2:p.Thr587Ser
ENST00000493795.5:c.4930A>T	ENSP00000418775.1:p.Thr1644Ser
ENST00000493919.5:c.1621A>T	ENSP00000418819.1:p.Thr541Ser
ENST00000586385.5:c.5-3660A>T	ENSP00000465818.1:n.5-3660A>T
ENST00000591534.5:c.544A>T	ENSP00000467329.1:p.Thr182Ser
ENST00000591849.5:c.-98-17421A>T	ENSP00000465347.1:n.-98-17421A>T
NM_007294.3:c.5071A>T , LRG_292t1:c.5071A>T	NP_009225.1:p.Thr1691Ser
NM_007297.3:c.4930A>T	NP_009228.2:p.Thr1644Ser
NM_007298.3:c.1759A>T	NP_009229.2:p.Thr587Ser
NM_007299.3:c.1759A>T	NP_009230.2:p.Thr587Ser
NM_007300.3:c.5134A>T	NP_009231.2:p.Thr1712Ser
NR_027676.1:n.5207A>T
NM_007294.4:c.5071A>T MANE Select	NP_009225.1:p.Thr1691Ser
NM_007297.4:c.4930A>T	NP_009228.2:p.Thr1644Ser
NM_007299.4:c.1759A>T	NP_009230.2:p.Thr587Ser
NM_007300.4:c.5134A>T	NP_009231.2:p.Thr1712Ser
NR_027676.2:n.5248A>T