Canonical Allele Identifier: CA10594191

Gene: BRCA1

Linked Data

• ClinVar Variation Id: 658764
• ClinVar RCV Id: RCV000815649 ; RCV003158216
• dbSNP Id: rs1597860658
• MyVariant Identifiers: chr17:g.41243662A>G (hg19) ; chr17:g.43091645A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43091645A>G , CM000679.2:g.43091645A>G	GRCh38
NC_000017.10:g.41243662A>G , CM000679.1:g.41243662A>G	GRCh37
NC_000017.9:g.38497188A>G	NCBI36
NG_005905.2:g.126339T>C , LRG_292:g.126339T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354071.8:n.3950T>C
ENST00000461574.2:c.3886T>C	ENSP00000417241.2:p.Phe1296Leu
ENST00000470026.6:c.3886T>C	ENSP00000419274.2:p.Phe1296Leu
ENST00000473961.6:c.3760T>C	ENSP00000420201.2:p.Phe1254Leu
ENST00000476777.6:c.3883T>C	ENSP00000417554.2:p.Phe1295Leu
ENST00000477152.6:c.3808T>C	ENSP00000419988.2:p.Phe1270Leu
ENST00000478531.6:c.785-613T>C	ENSP00000420412.2:n.785-613T>C
ENST00000489037.2:c.3808T>C	ENSP00000420781.2:p.Phe1270Leu
ENST00000493919.6:c.647-613T>C	ENSP00000418819.2:n.647-613T>C
ENST00000494123.6:c.3886T>C	ENSP00000419103.2:p.Phe1296Leu
ENST00000497488.2:c.2998T>C	ENSP00000418986.2:p.Phe1000Leu
ENST00000618469.2:c.3886T>C	ENSP00000478114.2:p.Phe1296Leu
ENST00000634433.2:c.3763T>C	ENSP00000489431.2:p.Phe1255Leu
ENST00000644379.2:c.3886T>C	ENSP00000496570.2:p.Phe1296Leu
ENST00000644555.2:c.647-613T>C	ENSP00000494614.2:n.647-613T>C
ENST00000652672.2:c.3745T>C	ENSP00000498906.2:p.Phe1249Leu
ENST00000484087.6:c.665-613T>C	ENSP00000419481.2:n.665-613T>C
ENST00000700182.1:c.707-613T>C	ENSP00000514849.1:n.707-613T>C
ENST00000357654.9:c.3886T>C MANE Select	ENSP00000350283.3:p.Phe1296Leu
ENST00000471181.7:c.3886T>C	ENSP00000418960.2:p.Phe1296Leu
ENST00000644379.1:c.207T>C
ENST00000352993.7:c.671-613T>C	ENSP00000312236.5:n.671-613T>C
ENST00000354071.7:c.3886T>C	ENSP00000326002.7:p.Phe1296Leu
ENST00000357654.7:c.3886T>C	ENSP00000350283.3:p.Phe1296Leu
ENST00000461221.5:c.*3669T>C	ENSP00000418548.1:n.*3669T>C
ENST00000461574.1:c.180T>C
ENST00000468300.5:c.788-613T>C	ENSP00000417148.1:n.788-613T>C
ENST00000471181.6:c.3886T>C	ENSP00000418960.2:p.Phe1296Leu
ENST00000478531.5:c.785-613T>C	ENSP00000420412.1:n.785-613T>C
ENST00000484087.5:c.410-613T>C	ENSP00000419481.1:n.410-613T>C
ENST00000487825.5:c.413-613T>C	ENSP00000418212.1:n.413-613T>C
ENST00000491747.6:c.788-613T>C	ENSP00000420705.2:n.788-613T>C
ENST00000493795.5:c.3745T>C	ENSP00000418775.1:p.Phe1249Leu
ENST00000493919.5:c.647-613T>C	ENSP00000418819.1:n.647-613T>C
ENST00000586385.5:c.5-27694T>C	ENSP00000465818.1:n.5-27694T>C
ENST00000591534.5:c.-43-17124T>C	ENSP00000467329.1:n.-43-17124T>C
ENST00000591849.5:c.-99+33626T>C	ENSP00000465347.1:n.-99+33626T>C
NM_007294.3:c.3886T>C , LRG_292t1:c.3886T>C	NP_009225.1:p.Phe1296Leu
NM_007297.3:c.3745T>C	NP_009228.2:p.Phe1249Leu
NM_007298.3:c.788-613T>C	NP_009229.2:n.788-613T>C
NM_007299.3:c.788-613T>C	NP_009230.2:n.788-613T>C
NM_007300.3:c.3886T>C	NP_009231.2:p.Phe1296Leu
NR_027676.1:n.4022T>C
NM_007294.4:c.3886T>C MANE Select	NP_009225.1:p.Phe1296Leu
NM_007297.4:c.3745T>C	NP_009228.2:p.Phe1249Leu
NM_007299.4:c.788-613T>C	NP_009230.2:n.788-613T>C
NM_007300.4:c.3886T>C	NP_009231.2:p.Phe1296Leu
NR_027676.2:n.4063T>C