Canonical Allele Identifier: CA10594485

Gene: BRCA1

Linked Data

• ClinVar Variation Id: 1063293
• ClinVar RCV Id: RCV001373118 ; RCV003158889
• dbSNP Id: rs2053534351
• MyVariant Identifiers: chr17:g.41243806C>T (hg19) ; chr17:g.43091789C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43091789C>T , CM000679.2:g.43091789C>T	GRCh38
NC_000017.10:g.41243806C>T , CM000679.1:g.41243806C>T	GRCh37
NC_000017.9:g.38497332C>T	NCBI36
NG_005905.2:g.126195G>A , LRG_292:g.126195G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000354071.8:n.3806G>A
ENST00000461574.2:c.3742G>A	ENSP00000417241.2:p.Ala1248Thr
ENST00000470026.6:c.3742G>A	ENSP00000419274.2:p.Ala1248Thr
ENST00000473961.6:c.3616G>A	ENSP00000420201.2:p.Ala1206Thr
ENST00000476777.6:c.3739G>A	ENSP00000417554.2:p.Ala1247Thr
ENST00000477152.6:c.3664G>A	ENSP00000419988.2:p.Ala1222Thr
ENST00000478531.6:c.785-757G>A	ENSP00000420412.2:n.785-757G>A
ENST00000489037.2:c.3664G>A	ENSP00000420781.2:p.Ala1222Thr
ENST00000493919.6:c.647-757G>A	ENSP00000418819.2:n.647-757G>A
ENST00000494123.6:c.3742G>A	ENSP00000419103.2:p.Ala1248Thr
ENST00000497488.2:c.2854G>A	ENSP00000418986.2:p.Ala952Thr
ENST00000618469.2:c.3742G>A	ENSP00000478114.2:p.Ala1248Thr
ENST00000634433.2:c.3619G>A	ENSP00000489431.2:p.Ala1207Thr
ENST00000644379.2:c.3742G>A	ENSP00000496570.2:p.Ala1248Thr
ENST00000644555.2:c.647-757G>A	ENSP00000494614.2:n.647-757G>A
ENST00000652672.2:c.3601G>A	ENSP00000498906.2:p.Ala1201Thr
ENST00000484087.6:c.665-757G>A	ENSP00000419481.2:n.665-757G>A
ENST00000700182.1:c.707-757G>A	ENSP00000514849.1:n.707-757G>A
ENST00000357654.9:c.3742G>A MANE Select	ENSP00000350283.3:p.Ala1248Thr
ENST00000471181.7:c.3742G>A	ENSP00000418960.2:p.Ala1248Thr
ENST00000644379.1:c.63G>A
ENST00000352993.7:c.671-757G>A	ENSP00000312236.5:n.671-757G>A
ENST00000354071.7:c.3742G>A	ENSP00000326002.7:p.Ala1248Thr
ENST00000357654.7:c.3742G>A	ENSP00000350283.3:p.Ala1248Thr
ENST00000461221.5:c.*3525G>A	ENSP00000418548.1:n.*3525G>A
ENST00000461574.1:c.36G>A
ENST00000468300.5:c.788-757G>A	ENSP00000417148.1:n.788-757G>A
ENST00000471181.6:c.3742G>A	ENSP00000418960.2:p.Ala1248Thr
ENST00000478531.5:c.785-757G>A	ENSP00000420412.1:n.785-757G>A
ENST00000484087.5:c.410-757G>A	ENSP00000419481.1:n.410-757G>A
ENST00000487825.5:c.413-757G>A	ENSP00000418212.1:n.413-757G>A
ENST00000491747.6:c.788-757G>A	ENSP00000420705.2:n.788-757G>A
ENST00000493795.5:c.3601G>A	ENSP00000418775.1:p.Ala1201Thr
ENST00000493919.5:c.647-757G>A	ENSP00000418819.1:n.647-757G>A
ENST00000586385.5:c.5-27838G>A	ENSP00000465818.1:n.5-27838G>A
ENST00000591534.5:c.-43-17268G>A	ENSP00000467329.1:n.-43-17268G>A
ENST00000591849.5:c.-99+33482G>A	ENSP00000465347.1:n.-99+33482G>A
NM_007294.3:c.3742G>A , LRG_292t1:c.3742G>A	NP_009225.1:p.Ala1248Thr
NM_007297.3:c.3601G>A	NP_009228.2:p.Ala1201Thr
NM_007298.3:c.788-757G>A	NP_009229.2:n.788-757G>A
NM_007299.3:c.788-757G>A	NP_009230.2:n.788-757G>A
NM_007300.3:c.3742G>A	NP_009231.2:p.Ala1248Thr
NR_027676.1:n.3878G>A
NM_007294.4:c.3742G>A MANE Select	NP_009225.1:p.Ala1248Thr
NM_007297.4:c.3601G>A	NP_009228.2:p.Ala1201Thr
NM_007299.4:c.788-757G>A	NP_009230.2:n.788-757G>A
NM_007300.4:c.3742G>A	NP_009231.2:p.Ala1248Thr
NR_027676.2:n.3919G>A