Canonical Allele Identifier: CA002723

Gene: BRCA1

Linked Data

• ClinVar Variation Id: 55147
• ClinVar RCV Id: RCV000112302 ; RCV001294633 ; RCV001022101
• dbSNP Id: rs273900729
• MyVariant Identifiers: chr17:g.41234546A>G (hg19) ; chr17:g.43082529A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43082529A>G , CM000679.2:g.43082529A>G	GRCh38
NC_000017.10:g.41234546A>G , CM000679.1:g.41234546A>G	GRCh37
NC_000017.9:g.38488072A>G	NCBI36
NG_005905.2:g.135455T>C , LRG_292:g.135455T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461574.2:c.4232T>C	ENSP00000417241.2:p.Met1411Thr
ENST00000470026.6:c.4232T>C	ENSP00000419274.2:p.Met1411Thr
ENST00000473961.6:c.4106T>C	ENSP00000420201.2:p.Met1369Thr
ENST00000476777.6:c.4226T>C	ENSP00000417554.2:p.Met1409Thr
ENST00000477152.6:c.4154T>C	ENSP00000419988.2:p.Met1385Thr
ENST00000478531.6:c.920T>C	ENSP00000420412.2:p.Met307Thr
ENST00000489037.2:c.4154T>C	ENSP00000420781.2:p.Met1385Thr
ENST00000493919.6:c.782T>C	ENSP00000418819.2:p.Met261Thr
ENST00000494123.6:c.4232T>C	ENSP00000419103.2:p.Met1411Thr
ENST00000497488.2:c.3344T>C	ENSP00000418986.2:p.Met1115Thr
ENST00000618469.2:c.4232T>C	ENSP00000478114.2:p.Met1411Thr
ENST00000634433.2:c.4109T>C	ENSP00000489431.2:p.Met1370Thr
ENST00000644379.2:c.4232T>C	ENSP00000496570.2:p.Met1411Thr
ENST00000644555.2:c.782T>C	ENSP00000494614.2:p.Met261Thr
ENST00000652672.2:c.4091T>C	ENSP00000498906.2:p.Met1364Thr
ENST00000484087.6:c.797T>C	ENSP00000419481.2:p.Met266Thr
ENST00000700182.1:c.842T>C	ENSP00000514849.1:p.Met281Thr
ENST00000357654.9:c.4232T>C MANE Select	ENSP00000350283.3:p.Met1411Thr
ENST00000471181.7:c.4232T>C	ENSP00000418960.2:p.Met1411Thr
ENST00000644379.1:c.553T>C
ENST00000352993.7:c.806T>C	ENSP00000312236.5:p.Met269Thr
ENST00000357654.7:c.4232T>C	ENSP00000350283.3:p.Met1411Thr
ENST00000461221.5:c.*4015T>C	ENSP00000418548.1:n.*4015T>C
ENST00000461574.1:c.526T>C
ENST00000468300.5:c.923T>C	ENSP00000417148.1:p.Met308Thr
ENST00000471181.6:c.4232T>C	ENSP00000418960.2:p.Met1411Thr
ENST00000478531.5:c.920T>C	ENSP00000420412.1:p.Met307Thr
ENST00000484087.5:c.545T>C	ENSP00000419481.1:p.Met182Thr
ENST00000487825.5:c.548T>C	ENSP00000418212.1:p.Met183Thr
ENST00000491747.6:c.923T>C	ENSP00000420705.2:p.Met308Thr
ENST00000493795.5:c.4091T>C	ENSP00000418775.1:p.Met1364Thr
ENST00000493919.5:c.782T>C	ENSP00000418819.1:p.Met261Thr
ENST00000586385.5:c.5-18578T>C	ENSP00000465818.1:n.5-18578T>C
ENST00000591534.5:c.-43-8008T>C	ENSP00000467329.1:n.-43-8008T>C
ENST00000591849.5:c.-98-32339T>C	ENSP00000465347.1:n.-98-32339T>C
ENST00000621897.1:n.126T>C
NM_007294.3:c.4232T>C , LRG_292t1:c.4232T>C	NP_009225.1:p.Met1411Thr
NM_007297.3:c.4091T>C	NP_009228.2:p.Met1364Thr
NM_007298.3:c.923T>C	NP_009229.2:p.Met308Thr
NM_007299.3:c.923T>C	NP_009230.2:p.Met308Thr
NM_007300.3:c.4232T>C	NP_009231.2:p.Met1411Thr
NR_027676.1:n.4368T>C
NM_007294.4:c.4232T>C MANE Select	NP_009225.1:p.Met1411Thr
NM_007297.4:c.4091T>C	NP_009228.2:p.Met1364Thr
NM_007299.4:c.923T>C	NP_009230.2:p.Met308Thr
NM_007300.4:c.4232T>C	NP_009231.2:p.Met1411Thr
NR_027676.2:n.4409T>C