Canonical Allele Identifier: CA001588

Gene: BRCA1

Linked Data

• ClinVar Variation Id: 17682
• ClinVar RCV Id: RCV000019252 ; RCV000212169 ; RCV000162856 ; RCV000496416 ; RCV000769717
• dbSNP Id: rs62625306
• gnomAD v4: 17-43093142-C-A
• MyVariant Identifiers: chr17:g.41245159C>A (hg19) ; chr17:g.43093142C>A (hg38)
• PubMed: PMID:9585617 ; PMID:21990299

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43093142C>A , CM000679.2:g.43093142C>A	GRCh38
NC_000017.10:g.41245159C>A , CM000679.1:g.41245159C>A	GRCh37
NC_000017.9:g.38498685C>A	NCBI36
NG_005905.2:g.124842G>T , LRG_292:g.124842G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354071.8:n.2453G>T
ENST00000461574.2:c.2389G>T	ENSP00000417241.2:p.Glu797Ter
ENST00000470026.6:c.2389G>T	ENSP00000419274.2:p.Glu797Ter
ENST00000473961.6:c.2263G>T	ENSP00000420201.2:p.Glu755Ter
ENST00000476777.6:c.2386G>T	ENSP00000417554.2:p.Glu796Ter
ENST00000477152.6:c.2311G>T	ENSP00000419988.2:p.Glu771Ter
ENST00000478531.6:c.784+1602G>T	ENSP00000420412.2:n.784+1602G>T
ENST00000489037.2:c.2311G>T	ENSP00000420781.2:p.Glu771Ter
ENST00000493919.6:c.646+1602G>T	ENSP00000418819.2:n.646+1602G>T
ENST00000494123.6:c.2389G>T	ENSP00000419103.2:p.Glu797Ter
ENST00000497488.2:c.1501G>T	ENSP00000418986.2:p.Glu501Ter
ENST00000618469.2:c.2389G>T	ENSP00000478114.2:p.Glu797Ter
ENST00000634433.2:c.2266G>T	ENSP00000489431.2:p.Glu756Ter
ENST00000644379.2:c.2389G>T	ENSP00000496570.2:p.Glu797Ter
ENST00000644555.2:c.646+1602G>T	ENSP00000494614.2:n.646+1602G>T
ENST00000652672.2:c.2248G>T	ENSP00000498906.2:p.Glu750Ter
ENST00000484087.6:c.664+1602G>T	ENSP00000419481.2:n.664+1602G>T
ENST00000700182.1:c.706+1602G>T	ENSP00000514849.1:n.706+1602G>T
ENST00000357654.9:c.2389G>T MANE Select	ENSP00000350283.3:p.Glu797Ter
ENST00000471181.7:c.2389G>T	ENSP00000418960.2:p.Glu797Ter
ENST00000352993.7:c.671-2110G>T	ENSP00000312236.5:n.671-2110G>T
ENST00000354071.7:c.2389G>T	ENSP00000326002.7:p.Glu797Ter
ENST00000357654.7:c.2389G>T	ENSP00000350283.3:p.Glu797Ter
ENST00000461221.5:c.*2172G>T	ENSP00000418548.1:n.*2172G>T
ENST00000468300.5:c.787+1602G>T	ENSP00000417148.1:n.787+1602G>T
ENST00000471181.6:c.2389G>T	ENSP00000418960.2:p.Glu797Ter
ENST00000478531.5:c.784+1602G>T	ENSP00000420412.1:n.784+1602G>T
ENST00000484087.5:c.409+1602G>T	ENSP00000419481.1:n.409+1602G>T
ENST00000487825.5:c.412+1602G>T	ENSP00000418212.1:n.412+1602G>T
ENST00000491747.6:c.787+1602G>T	ENSP00000420705.2:n.787+1602G>T
ENST00000493795.5:c.2248G>T	ENSP00000418775.1:p.Glu750Ter
ENST00000493919.5:c.646+1602G>T	ENSP00000418819.1:n.646+1602G>T
ENST00000586385.5:c.5-29191G>T	ENSP00000465818.1:n.5-29191G>T
ENST00000591534.5:c.-43-18621G>T	ENSP00000467329.1:n.-43-18621G>T
ENST00000591849.5:c.-99+32129G>T	ENSP00000465347.1:n.-99+32129G>T
ENST00000634433.1:c.2266G>T	ENSP00000489431.1:p.Glu756Ter
NM_007294.3:c.2389G>T , LRG_292t1:c.2389G>T	NP_009225.1:p.Glu797Ter
NM_007297.3:c.2248G>T	NP_009228.2:p.Glu750Ter
NM_007298.3:c.787+1602G>T	NP_009229.2:n.787+1602G>T
NM_007299.3:c.787+1602G>T	NP_009230.2:n.787+1602G>T
NM_007300.3:c.2389G>T	NP_009231.2:p.Glu797Ter
NR_027676.1:n.2525G>T
NM_007294.4:c.2389G>T MANE Select	NP_009225.1:p.Glu797Ter
NM_007297.4:c.2248G>T	NP_009228.2:p.Glu750Ter
NM_007299.4:c.787+1602G>T	NP_009230.2:n.787+1602G>T
NM_007300.4:c.2389G>T	NP_009231.2:p.Glu797Ter
NR_027676.2:n.2566G>T