Canonical Allele Identifier: CA001760

Gene: BRCA1

Linked Data

• ClinVar Variation Id: 54642
• ClinVar RCV Id: RCV000047926 ; RCV000112171 ; RCV000223325 ; RCV003493428
• dbSNP Id: rs80356963
• gnomAD v2: 17-41256919-G-C
• gnomAD v3: 17-43104902-G-C
• gnomAD v4: 17-43104902-G-C
• MyVariant Identifiers: chr17:g.41256919G>C (hg19) ; chr17:g.43104902G>C (hg38)
• PubMed: PMID:10923033

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43104902G>C , CM000679.2:g.43104902G>C	GRCh38
NC_000017.10:g.41256919G>C , CM000679.1:g.41256919G>C	GRCh37
NC_000017.9:g.38510445G>C	NCBI36
NG_005905.2:g.113082C>G , LRG_292:g.113082C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354071.8:n.331C>G
ENST00000461574.2:c.267C>G	ENSP00000417241.2:p.Ile89Met
ENST00000470026.6:c.267C>G	ENSP00000419274.2:p.Ile89Met
ENST00000473961.6:c.267C>G	ENSP00000420201.2:p.Ile89Met
ENST00000476777.6:c.267C>G	ENSP00000417554.2:p.Ile89Met
ENST00000477152.6:c.189C>G	ENSP00000419988.2:p.Ile63Met
ENST00000478531.6:c.267C>G	ENSP00000420412.2:p.Ile89Met
ENST00000489037.2:c.189C>G	ENSP00000420781.2:p.Ile63Met
ENST00000493919.6:c.126C>G	ENSP00000418819.2:p.Ile42Met
ENST00000494123.6:c.267C>G	ENSP00000419103.2:p.Ile89Met
ENST00000497488.2:c.-218-10042C>G	ENSP00000418986.2:n.-218-10042C>G
ENST00000618469.2:c.267C>G	ENSP00000478114.2:p.Ile89Met
ENST00000634433.2:c.267C>G	ENSP00000489431.2:p.Ile89Met
ENST00000644379.2:c.267C>G	ENSP00000496570.2:p.Ile89Met
ENST00000644555.2:c.126C>G	ENSP00000494614.2:p.Ile42Met
ENST00000652672.2:c.126C>G	ENSP00000498906.2:p.Ile42Met
ENST00000484087.6:c.267C>G	ENSP00000419481.2:p.Ile89Met
ENST00000700083.1:n.1238C>G
ENST00000700182.1:c.189C>G	ENSP00000514849.1:p.Ile63Met
ENST00000700183.1:c.*181C>G	ENSP00000514850.1:n.*181C>G
ENST00000700184.1:n.510C>G
ENST00000357654.9:c.267C>G MANE Select	ENSP00000350283.3:p.Ile89Met
ENST00000471181.7:c.267C>G	ENSP00000418960.2:p.Ile89Met
ENST00000642945.1:c.*141C>G	ENSP00000495897.1:n.*141C>G
ENST00000644555.1:c.126C>G	ENSP00000494614.1:p.Ile42Met
ENST00000652672.1:c.126C>G	ENSP00000498906.1:p.Ile42Met
ENST00000352993.7:c.267C>G	ENSP00000312236.5:p.Ile89Met
ENST00000354071.7:c.267C>G	ENSP00000326002.7:p.Ile89Met
ENST00000357654.7:c.267C>G	ENSP00000350283.3:p.Ile89Met
ENST00000461221.5:c.*53C>G	ENSP00000418548.1:n.*53C>G
ENST00000461798.5:c.*53C>G	ENSP00000417988.1:n.*53C>G
ENST00000468300.5:c.267C>G	ENSP00000417148.1:p.Ile89Met
ENST00000470026.5:c.267C>G	ENSP00000419274.1:p.Ile89Met
ENST00000471181.6:c.267C>G	ENSP00000418960.2:p.Ile89Met
ENST00000476777.5:c.267C>G	ENSP00000417554.1:p.Ile89Met
ENST00000477152.5:c.189C>G	ENSP00000419988.1:p.Ile63Met
ENST00000478531.5:c.267C>G	ENSP00000420412.1:p.Ile89Met
ENST00000484087.5:c.15C>G	ENSP00000419481.1:p.Ile5Met
ENST00000487825.5:c.15C>G	ENSP00000418212.1:p.Ile5Met
ENST00000489037.1:c.189C>G	ENSP00000420781.1:p.Ile63Met
ENST00000491747.6:c.267C>G	ENSP00000420705.2:p.Ile89Met
ENST00000492859.5:c.*203C>G	ENSP00000420253.1:n.*203C>G
ENST00000493795.5:c.126C>G	ENSP00000418775.1:p.Ile42Met
ENST00000493919.5:c.126C>G	ENSP00000418819.1:p.Ile42Met
ENST00000494123.5:c.267C>G	ENSP00000419103.1:p.Ile89Met
ENST00000497488.1:c.-218-10042C>G	ENSP00000418986.1:n.-218-10042C>G
ENST00000586385.5:c.4+20280C>G	ENSP00000465818.1:n.4+20280C>G
ENST00000591534.5:c.-44+20369C>G	ENSP00000467329.1:n.-44+20369C>G
ENST00000591849.5:c.-99+20369C>G	ENSP00000465347.1:n.-99+20369C>G
ENST00000634433.1:c.267C>G	ENSP00000489431.1:p.Ile89Met
NM_007294.3:c.267C>G , LRG_292t1:c.267C>G	NP_009225.1:p.Ile89Met
NM_007297.3:c.126C>G	NP_009228.2:p.Ile42Met
NM_007298.3:c.267C>G	NP_009229.2:p.Ile89Met
NM_007299.3:c.267C>G	NP_009230.2:p.Ile89Met
NM_007300.3:c.267C>G	NP_009231.2:p.Ile89Met
NR_027676.1:n.406C>G
NM_007294.4:c.267C>G MANE Select	NP_009225.1:p.Ile89Met
NM_007297.4:c.126C>G	NP_009228.2:p.Ile42Met
NM_007299.4:c.267C>G	NP_009230.2:p.Ile89Met
NM_007300.4:c.267C>G	NP_009231.2:p.Ile89Met
NR_027676.2:n.447C>G