Canonical Allele Identifier: CA10592613

Gene: BRCA1

Linked Data

• MyVariant Identifiers: chr17:g.41228528T>G (hg19) ; chr17:g.43076511T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43076511T>G , CM000679.2:g.43076511T>G	GRCh38
NC_000017.10:g.41228528T>G , CM000679.1:g.41228528T>G	GRCh37
NC_000017.9:g.38482054T>G	NCBI36
NG_005905.2:g.141473A>C , LRG_292:g.141473A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000461574.2:c.4458A>C	ENSP00000417241.2:p.Lys1486Asn
ENST00000470026.6:c.4461A>C	ENSP00000419274.2:p.Lys1487Asn
ENST00000473961.6:c.4335A>C	ENSP00000420201.2:p.Lys1445Asn
ENST00000476777.6:c.4455A>C	ENSP00000417554.2:p.Lys1485Asn
ENST00000477152.6:c.4383A>C	ENSP00000419988.2:p.Lys1461Asn
ENST00000478531.6:c.1149A>C	ENSP00000420412.2:p.Lys383Asn
ENST00000489037.2:c.4383A>C	ENSP00000420781.2:p.Lys1461Asn
ENST00000493919.6:c.1011A>C	ENSP00000418819.2:p.Lys337Asn
ENST00000494123.6:c.4461A>C	ENSP00000419103.2:p.Lys1487Asn
ENST00000497488.2:c.3573A>C	ENSP00000418986.2:p.Lys1191Asn
ENST00000618469.2:c.4461A>C	ENSP00000478114.2:p.Lys1487Asn
ENST00000634433.2:c.4338A>C	ENSP00000489431.2:p.Lys1446Asn
ENST00000644379.2:c.4527A>C	ENSP00000496570.2:p.Lys1509Asn
ENST00000644555.2:c.1011A>C	ENSP00000494614.2:p.Lys337Asn
ENST00000652672.2:c.4320A>C	ENSP00000498906.2:p.Lys1440Asn
ENST00000484087.6:c.1023A>C	ENSP00000419481.2:p.Lys341Asn
ENST00000700182.1:c.1068A>C	ENSP00000514849.1:p.Lys356Asn
ENST00000357654.9:c.4461A>C MANE Select	ENSP00000350283.3:p.Lys1487Asn
ENST00000471181.7:c.4524A>C	ENSP00000418960.2:p.Lys1508Asn
ENST00000644379.1:c.848A>C
ENST00000352993.7:c.1035A>C	ENSP00000312236.5:p.Lys345Asn
ENST00000357654.7:c.4461A>C	ENSP00000350283.3:p.Lys1487Asn
ENST00000461221.5:c.*4244A>C	ENSP00000418548.1:n.*4244A>C
ENST00000468300.5:c.1149A>C	ENSP00000417148.1:p.Lys383Asn
ENST00000471181.6:c.4524A>C	ENSP00000418960.2:p.Lys1508Asn
ENST00000478531.5:c.1149A>C	ENSP00000420412.1:p.Lys383Asn
ENST00000484087.5:c.774A>C	ENSP00000419481.1:p.Lys258Asn
ENST00000487825.5:c.777A>C	ENSP00000418212.1:p.Lys259Asn
ENST00000491747.6:c.1149A>C	ENSP00000420705.2:p.Lys383Asn
ENST00000493795.5:c.4320A>C	ENSP00000418775.1:p.Lys1440Asn
ENST00000493919.5:c.1011A>C	ENSP00000418819.1:p.Lys337Asn
ENST00000586385.5:c.5-12560A>C	ENSP00000465818.1:n.5-12560A>C
ENST00000591534.5:c.-43-1990A>C	ENSP00000467329.1:n.-43-1990A>C
ENST00000591849.5:c.-98-26321A>C	ENSP00000465347.1:n.-98-26321A>C
ENST00000621897.1:n.352A>C
NM_007294.3:c.4461A>C , LRG_292t1:c.4461A>C	NP_009225.1:p.Lys1487Asn
NM_007297.3:c.4320A>C	NP_009228.2:p.Lys1440Asn
NM_007298.3:c.1149A>C	NP_009229.2:p.Lys383Asn
NM_007299.3:c.1149A>C	NP_009230.2:p.Lys383Asn
NM_007300.3:c.4524A>C	NP_009231.2:p.Lys1508Asn
NR_027676.1:n.4597A>C
NM_007294.4:c.4461A>C MANE Select	NP_009225.1:p.Lys1487Asn
NM_007297.4:c.4320A>C	NP_009228.2:p.Lys1440Asn
NM_007299.4:c.1149A>C	NP_009230.2:p.Lys383Asn
NM_007300.4:c.4524A>C	NP_009231.2:p.Lys1508Asn
NR_027676.2:n.4638A>C