Canonical Allele Identifier: CA001104

Gene: BRCA1

Linked Data

• ClinVar Variation Id: 54323
• ClinVar RCV Id: RCV001852987 ; RCV003157334
• dbSNP Id: rs80356980
• MyVariant Identifiers: chr17:g.41245872C>A (hg19) ; chr17:g.43093855C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43093855C>A , CM000679.2:g.43093855C>A	GRCh38
NC_000017.10:g.41245872C>A , CM000679.1:g.41245872C>A	GRCh37
NC_000017.9:g.38499398C>A	NCBI36
NG_005905.2:g.124129G>T , LRG_292:g.124129G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000354071.8:n.1740G>T
ENST00000461574.2:c.1676G>T	ENSP00000417241.2:p.Gly559Val
ENST00000470026.6:c.1676G>T	ENSP00000419274.2:p.Gly559Val
ENST00000473961.6:c.1550G>T	ENSP00000420201.2:p.Gly517Val
ENST00000476777.6:c.1673G>T	ENSP00000417554.2:p.Gly558Val
ENST00000477152.6:c.1598G>T	ENSP00000419988.2:p.Gly533Val
ENST00000478531.6:c.784+889G>T	ENSP00000420412.2:n.784+889G>T
ENST00000489037.2:c.1598G>T	ENSP00000420781.2:p.Gly533Val
ENST00000493919.6:c.646+889G>T	ENSP00000418819.2:n.646+889G>T
ENST00000494123.6:c.1676G>T	ENSP00000419103.2:p.Gly559Val
ENST00000497488.2:c.788G>T	ENSP00000418986.2:p.Gly263Val
ENST00000618469.2:c.1676G>T	ENSP00000478114.2:p.Gly559Val
ENST00000634433.2:c.1553G>T	ENSP00000489431.2:p.Gly518Val
ENST00000644379.2:c.1676G>T	ENSP00000496570.2:p.Gly559Val
ENST00000644555.2:c.646+889G>T	ENSP00000494614.2:n.646+889G>T
ENST00000652672.2:c.1535G>T	ENSP00000498906.2:p.Gly512Val
ENST00000484087.6:c.664+889G>T	ENSP00000419481.2:n.664+889G>T
ENST00000700182.1:c.706+889G>T	ENSP00000514849.1:n.706+889G>T
ENST00000357654.9:c.1676G>T MANE Select	ENSP00000350283.3:p.Gly559Val
ENST00000471181.7:c.1676G>T	ENSP00000418960.2:p.Gly559Val
ENST00000652672.1:c.1535G>T	ENSP00000498906.1:p.Gly512Val
ENST00000352993.7:c.670+1991G>T	ENSP00000312236.5:n.670+1991G>T
ENST00000354071.7:c.1676G>T	ENSP00000326002.7:p.Gly559Val
ENST00000357654.7:c.1676G>T	ENSP00000350283.3:p.Gly559Val
ENST00000412061.3:c.1027G>T
ENST00000461221.5:c.*1459G>T	ENSP00000418548.1:n.*1459G>T
ENST00000468300.5:c.787+889G>T	ENSP00000417148.1:n.787+889G>T
ENST00000470026.5:c.1676G>T	ENSP00000419274.1:p.Gly559Val
ENST00000471181.6:c.1676G>T	ENSP00000418960.2:p.Gly559Val
ENST00000477152.5:c.1598G>T	ENSP00000419988.1:p.Gly533Val
ENST00000478531.5:c.784+889G>T	ENSP00000420412.1:n.784+889G>T
ENST00000484087.5:c.409+889G>T	ENSP00000419481.1:n.409+889G>T
ENST00000487825.5:c.412+889G>T	ENSP00000418212.1:n.412+889G>T
ENST00000491747.6:c.787+889G>T	ENSP00000420705.2:n.787+889G>T
ENST00000493795.5:c.1535G>T	ENSP00000418775.1:p.Gly512Val
ENST00000493919.5:c.646+889G>T	ENSP00000418819.1:n.646+889G>T
ENST00000586385.5:c.5-29904G>T	ENSP00000465818.1:n.5-29904G>T
ENST00000591534.5:c.-43-19334G>T	ENSP00000467329.1:n.-43-19334G>T
ENST00000591849.5:c.-99+31416G>T	ENSP00000465347.1:n.-99+31416G>T
ENST00000634433.1:c.1553G>T	ENSP00000489431.1:p.Gly518Val
NM_007294.3:c.1676G>T , LRG_292t1:c.1676G>T	NP_009225.1:p.Gly559Val
NM_007297.3:c.1535G>T	NP_009228.2:p.Gly512Val
NM_007298.3:c.787+889G>T	NP_009229.2:n.787+889G>T
NM_007299.3:c.787+889G>T	NP_009230.2:n.787+889G>T
NM_007300.3:c.1676G>T	NP_009231.2:p.Gly559Val
NR_027676.1:n.1812G>T
NM_007294.4:c.1676G>T MANE Select	NP_009225.1:p.Gly559Val
NM_007297.4:c.1535G>T	NP_009228.2:p.Gly512Val
NM_007299.4:c.787+889G>T	NP_009230.2:n.787+889G>T
NM_007300.4:c.1676G>T	NP_009231.2:p.Gly559Val
NR_027676.2:n.1853G>T