Canonical Allele Identifier: CA10592629

Gene: BRCA1

Linked Data

• MyVariant Identifiers: chr17:g.41228536T>G (hg19) ; chr17:g.43076519T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43076519T>G , CM000679.2:g.43076519T>G	GRCh38
NC_000017.10:g.41228536T>G , CM000679.1:g.41228536T>G	GRCh37
NC_000017.9:g.38482062T>G	NCBI36
NG_005905.2:g.141465A>C , LRG_292:g.141465A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000461574.2:c.4450A>C	ENSP00000417241.2:p.Thr1484Pro
ENST00000470026.6:c.4453A>C	ENSP00000419274.2:p.Thr1485Pro
ENST00000473961.6:c.4327A>C	ENSP00000420201.2:p.Thr1443Pro
ENST00000476777.6:c.4447A>C	ENSP00000417554.2:p.Thr1483Pro
ENST00000477152.6:c.4375A>C	ENSP00000419988.2:p.Thr1459Pro
ENST00000478531.6:c.1141A>C	ENSP00000420412.2:p.Thr381Pro
ENST00000489037.2:c.4375A>C	ENSP00000420781.2:p.Thr1459Pro
ENST00000493919.6:c.1003A>C	ENSP00000418819.2:p.Thr335Pro
ENST00000494123.6:c.4453A>C	ENSP00000419103.2:p.Thr1485Pro
ENST00000497488.2:c.3565A>C	ENSP00000418986.2:p.Thr1189Pro
ENST00000618469.2:c.4453A>C	ENSP00000478114.2:p.Thr1485Pro
ENST00000634433.2:c.4330A>C	ENSP00000489431.2:p.Thr1444Pro
ENST00000644379.2:c.4519A>C	ENSP00000496570.2:p.Thr1507Pro
ENST00000644555.2:c.1003A>C	ENSP00000494614.2:p.Thr335Pro
ENST00000652672.2:c.4312A>C	ENSP00000498906.2:p.Thr1438Pro
ENST00000484087.6:c.1015A>C	ENSP00000419481.2:p.Thr339Pro
ENST00000700182.1:c.1060A>C	ENSP00000514849.1:p.Thr354Pro
ENST00000357654.9:c.4453A>C MANE Select	ENSP00000350283.3:p.Thr1485Pro
ENST00000471181.7:c.4516A>C	ENSP00000418960.2:p.Thr1506Pro
ENST00000644379.1:c.840A>C
ENST00000352993.7:c.1027A>C	ENSP00000312236.5:p.Thr343Pro
ENST00000357654.7:c.4453A>C	ENSP00000350283.3:p.Thr1485Pro
ENST00000461221.5:c.*4236A>C	ENSP00000418548.1:n.*4236A>C
ENST00000468300.5:c.1141A>C	ENSP00000417148.1:p.Thr381Pro
ENST00000471181.6:c.4516A>C	ENSP00000418960.2:p.Thr1506Pro
ENST00000478531.5:c.1141A>C	ENSP00000420412.1:p.Thr381Pro
ENST00000484087.5:c.766A>C	ENSP00000419481.1:p.Thr256Pro
ENST00000487825.5:c.769A>C	ENSP00000418212.1:p.Thr257Pro
ENST00000491747.6:c.1141A>C	ENSP00000420705.2:p.Thr381Pro
ENST00000493795.5:c.4312A>C	ENSP00000418775.1:p.Thr1438Pro
ENST00000493919.5:c.1003A>C	ENSP00000418819.1:p.Thr335Pro
ENST00000586385.5:c.5-12568A>C	ENSP00000465818.1:n.5-12568A>C
ENST00000591534.5:c.-43-1998A>C	ENSP00000467329.1:n.-43-1998A>C
ENST00000591849.5:c.-98-26329A>C	ENSP00000465347.1:n.-98-26329A>C
ENST00000621897.1:n.344A>C
NM_007294.3:c.4453A>C , LRG_292t1:c.4453A>C	NP_009225.1:p.Thr1485Pro
NM_007297.3:c.4312A>C	NP_009228.2:p.Thr1438Pro
NM_007298.3:c.1141A>C	NP_009229.2:p.Thr381Pro
NM_007299.3:c.1141A>C	NP_009230.2:p.Thr381Pro
NM_007300.3:c.4516A>C	NP_009231.2:p.Thr1506Pro
NR_027676.1:n.4589A>C
NM_007294.4:c.4453A>C MANE Select	NP_009225.1:p.Thr1485Pro
NM_007297.4:c.4312A>C	NP_009228.2:p.Thr1438Pro
NM_007299.4:c.1141A>C	NP_009230.2:p.Thr381Pro
NM_007300.4:c.4516A>C	NP_009231.2:p.Thr1506Pro
NR_027676.2:n.4630A>C