Canonical Allele Identifier: CA002359

Gene: BRCA1

Linked Data

• ClinVar Variation Id: 37540
• ClinVar RCV Id: RCV000112154 ; RCV000580523 ; RCV000985406 ; RCV001384592
• dbSNP Id: rs80357162
• MyVariant Identifiers: chr17:g.41243859A>C (hg19) ; chr17:g.43091842A>C (hg38)
• PubMed: PMID:23683081

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43091842A>C , CM000679.2:g.43091842A>C	GRCh38
NC_000017.10:g.41243859A>C , CM000679.1:g.41243859A>C	GRCh37
NC_000017.9:g.38497385A>C	NCBI36
NG_005905.2:g.126142T>G , LRG_292:g.126142T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354071.8:n.3753T>G
ENST00000461574.2:c.3689T>G	ENSP00000417241.2:p.Leu1230Ter
ENST00000470026.6:c.3689T>G	ENSP00000419274.2:p.Leu1230Ter
ENST00000473961.6:c.3563T>G	ENSP00000420201.2:p.Leu1188Ter
ENST00000476777.6:c.3686T>G	ENSP00000417554.2:p.Leu1229Ter
ENST00000477152.6:c.3611T>G	ENSP00000419988.2:p.Leu1204Ter
ENST00000478531.6:c.785-810T>G	ENSP00000420412.2:n.785-810T>G
ENST00000489037.2:c.3611T>G	ENSP00000420781.2:p.Leu1204Ter
ENST00000493919.6:c.647-810T>G	ENSP00000418819.2:n.647-810T>G
ENST00000494123.6:c.3689T>G	ENSP00000419103.2:p.Leu1230Ter
ENST00000497488.2:c.2801T>G	ENSP00000418986.2:p.Leu934Ter
ENST00000618469.2:c.3689T>G	ENSP00000478114.2:p.Leu1230Ter
ENST00000634433.2:c.3566T>G	ENSP00000489431.2:p.Leu1189Ter
ENST00000644379.2:c.3689T>G	ENSP00000496570.2:p.Leu1230Ter
ENST00000644555.2:c.647-810T>G	ENSP00000494614.2:n.647-810T>G
ENST00000652672.2:c.3548T>G	ENSP00000498906.2:p.Leu1183Ter
ENST00000484087.6:c.665-810T>G	ENSP00000419481.2:n.665-810T>G
ENST00000700182.1:c.707-810T>G	ENSP00000514849.1:n.707-810T>G
ENST00000357654.9:c.3689T>G MANE Select	ENSP00000350283.3:p.Leu1230Ter
ENST00000471181.7:c.3689T>G	ENSP00000418960.2:p.Leu1230Ter
ENST00000644379.1:c.10T>G
ENST00000352993.7:c.671-810T>G	ENSP00000312236.5:n.671-810T>G
ENST00000354071.7:c.3689T>G	ENSP00000326002.7:p.Leu1230Ter
ENST00000357654.7:c.3689T>G	ENSP00000350283.3:p.Leu1230Ter
ENST00000461221.5:c.*3472T>G	ENSP00000418548.1:n.*3472T>G
ENST00000468300.5:c.788-810T>G	ENSP00000417148.1:n.788-810T>G
ENST00000471181.6:c.3689T>G	ENSP00000418960.2:p.Leu1230Ter
ENST00000478531.5:c.785-810T>G	ENSP00000420412.1:n.785-810T>G
ENST00000484087.5:c.410-810T>G	ENSP00000419481.1:n.410-810T>G
ENST00000487825.5:c.413-810T>G	ENSP00000418212.1:n.413-810T>G
ENST00000491747.6:c.788-810T>G	ENSP00000420705.2:n.788-810T>G
ENST00000493795.5:c.3548T>G	ENSP00000418775.1:p.Leu1183Ter
ENST00000493919.5:c.647-810T>G	ENSP00000418819.1:n.647-810T>G
ENST00000586385.5:c.5-27891T>G	ENSP00000465818.1:n.5-27891T>G
ENST00000591534.5:c.-43-17321T>G	ENSP00000467329.1:n.-43-17321T>G
ENST00000591849.5:c.-99+33429T>G	ENSP00000465347.1:n.-99+33429T>G
NM_007294.3:c.3689T>G , LRG_292t1:c.3689T>G	NP_009225.1:p.Leu1230Ter
NM_007297.3:c.3548T>G	NP_009228.2:p.Leu1183Ter
NM_007298.3:c.788-810T>G	NP_009229.2:n.788-810T>G
NM_007299.3:c.788-810T>G	NP_009230.2:n.788-810T>G
NM_007300.3:c.3689T>G	NP_009231.2:p.Leu1230Ter
NR_027676.1:n.3825T>G
NM_007294.4:c.3689T>G MANE Select	NP_009225.1:p.Leu1230Ter
NM_007297.4:c.3548T>G	NP_009228.2:p.Leu1183Ter
NM_007299.4:c.788-810T>G	NP_009230.2:n.788-810T>G
NM_007300.4:c.3689T>G	NP_009231.2:p.Leu1230Ter
NR_027676.2:n.3866T>G