Canonical Allele Identifier: CA10596082

Gene: BRCA1

Linked Data

• ClinVar Variation Id: 3069231
• ClinVar RCV Id: RCV004007775
• dbSNP Id: rs2154350506
• MyVariant Identifiers: chr17:g.41244591A>G (hg19) ; chr17:g.43092574A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43092574A>G , CM000679.2:g.43092574A>G	GRCh38
NC_000017.10:g.41244591A>G , CM000679.1:g.41244591A>G	GRCh37
NC_000017.9:g.38498117A>G	NCBI36
NG_005905.2:g.125410T>C , LRG_292:g.125410T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354071.8:n.3021T>C
ENST00000461574.2:c.2957T>C	ENSP00000417241.2:p.Ile986Thr
ENST00000470026.6:c.2957T>C	ENSP00000419274.2:p.Ile986Thr
ENST00000473961.6:c.2831T>C	ENSP00000420201.2:p.Ile944Thr
ENST00000476777.6:c.2954T>C	ENSP00000417554.2:p.Ile985Thr
ENST00000477152.6:c.2879T>C	ENSP00000419988.2:p.Ile960Thr
ENST00000478531.6:c.785-1542T>C	ENSP00000420412.2:n.785-1542T>C
ENST00000489037.2:c.2879T>C	ENSP00000420781.2:p.Ile960Thr
ENST00000493919.6:c.647-1542T>C	ENSP00000418819.2:n.647-1542T>C
ENST00000494123.6:c.2957T>C	ENSP00000419103.2:p.Ile986Thr
ENST00000497488.2:c.2069T>C	ENSP00000418986.2:p.Ile690Thr
ENST00000618469.2:c.2957T>C	ENSP00000478114.2:p.Ile986Thr
ENST00000634433.2:c.2834T>C	ENSP00000489431.2:p.Ile945Thr
ENST00000644379.2:c.2957T>C	ENSP00000496570.2:p.Ile986Thr
ENST00000644555.2:c.647-1542T>C	ENSP00000494614.2:n.647-1542T>C
ENST00000652672.2:c.2816T>C	ENSP00000498906.2:p.Ile939Thr
ENST00000484087.6:c.665-1542T>C	ENSP00000419481.2:n.665-1542T>C
ENST00000700182.1:c.707-1542T>C	ENSP00000514849.1:n.707-1542T>C
ENST00000357654.9:c.2957T>C MANE Select	ENSP00000350283.3:p.Ile986Thr
ENST00000471181.7:c.2957T>C	ENSP00000418960.2:p.Ile986Thr
ENST00000352993.7:c.671-1542T>C	ENSP00000312236.5:n.671-1542T>C
ENST00000354071.7:c.2957T>C	ENSP00000326002.7:p.Ile986Thr
ENST00000357654.7:c.2957T>C	ENSP00000350283.3:p.Ile986Thr
ENST00000461221.5:c.*2740T>C	ENSP00000418548.1:n.*2740T>C
ENST00000468300.5:c.788-1542T>C	ENSP00000417148.1:n.788-1542T>C
ENST00000471181.6:c.2957T>C	ENSP00000418960.2:p.Ile986Thr
ENST00000478531.5:c.785-1542T>C	ENSP00000420412.1:n.785-1542T>C
ENST00000484087.5:c.410-1542T>C	ENSP00000419481.1:n.410-1542T>C
ENST00000487825.5:c.413-1542T>C	ENSP00000418212.1:n.413-1542T>C
ENST00000491747.6:c.788-1542T>C	ENSP00000420705.2:n.788-1542T>C
ENST00000493795.5:c.2816T>C	ENSP00000418775.1:p.Ile939Thr
ENST00000493919.5:c.647-1542T>C	ENSP00000418819.1:n.647-1542T>C
ENST00000586385.5:c.5-28623T>C	ENSP00000465818.1:n.5-28623T>C
ENST00000591534.5:c.-43-18053T>C	ENSP00000467329.1:n.-43-18053T>C
ENST00000591849.5:c.-99+32697T>C	ENSP00000465347.1:n.-99+32697T>C
NM_007294.3:c.2957T>C , LRG_292t1:c.2957T>C	NP_009225.1:p.Ile986Thr
NM_007297.3:c.2816T>C	NP_009228.2:p.Ile939Thr
NM_007298.3:c.788-1542T>C	NP_009229.2:n.788-1542T>C
NM_007299.3:c.788-1542T>C	NP_009230.2:n.788-1542T>C
NM_007300.3:c.2957T>C	NP_009231.2:p.Ile986Thr
NR_027676.1:n.3093T>C
NM_007294.4:c.2957T>C MANE Select	NP_009225.1:p.Ile986Thr
NM_007297.4:c.2816T>C	NP_009228.2:p.Ile939Thr
NM_007299.4:c.788-1542T>C	NP_009230.2:n.788-1542T>C
NM_007300.4:c.2957T>C	NP_009231.2:p.Ile986Thr
NR_027676.2:n.3134T>C