Canonical Allele Identifier: CA10591656

Gene: BRCA1

Linked Data

• ClinVar Variation Id: 868425
• ClinVar RCV Id: RCV001077323
• dbSNP Id: rs70953661
• MyVariant Identifiers: chr17:g.41222997C>T (hg19) ; chr17:g.43070980C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43070980C>T , CM000679.2:g.43070980C>T	GRCh38
NC_000017.10:g.41222997C>T , CM000679.1:g.41222997C>T	GRCh37
NC_000017.9:g.38476523C>T	NCBI36
NG_005905.2:g.147004G>A , LRG_292:g.147004G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000461574.2:c.4931G>A	ENSP00000417241.2:p.Arg1644Lys
ENST00000470026.6:c.4934G>A	ENSP00000419274.2:p.Arg1645Lys
ENST00000473961.6:c.4808G>A	ENSP00000420201.2:p.Arg1603Lys
ENST00000476777.6:c.4928G>A	ENSP00000417554.2:p.Arg1643Lys
ENST00000477152.6:c.4856G>A	ENSP00000419988.2:p.Arg1619Lys
ENST00000478531.6:c.1622G>A	ENSP00000420412.2:p.Arg541Lys
ENST00000489037.2:c.4856G>A	ENSP00000420781.2:p.Arg1619Lys
ENST00000493919.6:c.1484G>A	ENSP00000418819.2:p.Arg495Lys
ENST00000494123.6:c.4934G>A	ENSP00000419103.2:p.Arg1645Lys
ENST00000497488.2:c.4046G>A	ENSP00000418986.2:p.Arg1349Lys
ENST00000618469.2:c.4934G>A	ENSP00000478114.2:p.Arg1645Lys
ENST00000634433.2:c.4811G>A	ENSP00000489431.2:p.Arg1604Lys
ENST00000644379.2:c.5000G>A	ENSP00000496570.2:p.Arg1667Lys
ENST00000644555.2:c.1484G>A	ENSP00000494614.2:p.Arg495Lys
ENST00000652672.2:c.4793G>A	ENSP00000498906.2:p.Arg1598Lys
ENST00000484087.6:c.1496G>A	ENSP00000419481.2:p.Arg499Lys
ENST00000700182.1:c.1541G>A	ENSP00000514849.1:p.Arg514Lys
ENST00000357654.9:c.4934G>A MANE Select	ENSP00000350283.3:p.Arg1645Lys
ENST00000471181.7:c.4997G>A	ENSP00000418960.2:p.Arg1666Lys
ENST00000644379.1:c.1321G>A
ENST00000352993.7:c.1508G>A	ENSP00000312236.5:p.Arg503Lys
ENST00000357654.7:c.4934G>A	ENSP00000350283.3:p.Arg1645Lys
ENST00000461221.5:c.*4717G>A	ENSP00000418548.1:n.*4717G>A
ENST00000468300.5:c.1622G>A	ENSP00000417148.1:p.Arg541Lys
ENST00000471181.6:c.4997G>A	ENSP00000418960.2:p.Arg1666Lys
ENST00000472490.1:n.87G>A
ENST00000478531.5:c.1622G>A	ENSP00000420412.1:p.Arg541Lys
ENST00000484087.5:c.1247G>A	ENSP00000419481.1:p.Arg416Lys
ENST00000491747.6:c.1622G>A	ENSP00000420705.2:p.Arg541Lys
ENST00000493795.5:c.4793G>A	ENSP00000418775.1:p.Arg1598Lys
ENST00000493919.5:c.1484G>A	ENSP00000418819.1:p.Arg495Lys
ENST00000586385.5:c.5-7029G>A	ENSP00000465818.1:n.5-7029G>A
ENST00000591534.5:c.407G>A	ENSP00000467329.1:p.Arg136Lys
ENST00000591849.5:c.-98-20790G>A	ENSP00000465347.1:n.-98-20790G>A
NM_007294.3:c.4934G>A , LRG_292t1:c.4934G>A	NP_009225.1:p.Arg1645Lys
NM_007297.3:c.4793G>A	NP_009228.2:p.Arg1598Lys
NM_007298.3:c.1622G>A	NP_009229.2:p.Arg541Lys
NM_007299.3:c.1622G>A	NP_009230.2:p.Arg541Lys
NM_007300.3:c.4997G>A	NP_009231.2:p.Arg1666Lys
NR_027676.1:n.5070G>A
NM_007294.4:c.4934G>A MANE Select	NP_009225.1:p.Arg1645Lys
NM_007297.4:c.4793G>A	NP_009228.2:p.Arg1598Lys
NM_007299.4:c.1622G>A	NP_009230.2:p.Arg541Lys
NM_007300.4:c.4997G>A	NP_009231.2:p.Arg1666Lys
NR_027676.2:n.5111G>A