Canonical Allele Identifier: CA16615657

Gene: BRCA1

Linked Data

• ClinVar Variation Id: 415549
• ClinVar RCV Id: RCV001076296 ; RCV001446950
• dbSNP Id: rs1060504555
• MyVariant Identifiers: chr17:g.41219644A>C (hg19) ; chr17:g.43067627A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43067627A>C , CM000679.2:g.43067627A>C	GRCh38
NC_000017.10:g.41219644A>C , CM000679.1:g.41219644A>C	GRCh37
NC_000017.9:g.38473170A>C	NCBI36
NG_005905.2:g.150357T>G , LRG_292:g.150357T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461574.2:c.5052T>G	ENSP00000417241.2:p.Thr1684=
ENST00000470026.6:c.5055T>G	ENSP00000419274.2:p.Thr1685=
ENST00000473961.6:c.4929T>G	ENSP00000420201.2:p.Thr1643=
ENST00000476777.6:c.5049T>G	ENSP00000417554.2:p.Thr1683=
ENST00000477152.6:c.4977T>G	ENSP00000419988.2:p.Thr1659=
ENST00000478531.6:c.1743T>G	ENSP00000420412.2:p.Thr581=
ENST00000489037.2:c.4977T>G	ENSP00000420781.2:p.Thr1659=
ENST00000493919.6:c.1605T>G	ENSP00000418819.2:p.Thr535=
ENST00000494123.6:c.5055T>G	ENSP00000419103.2:p.Thr1685=
ENST00000497488.2:c.4167T>G	ENSP00000418986.2:p.Thr1389=
ENST00000618469.2:c.5055T>G	ENSP00000478114.2:p.Thr1685=
ENST00000634433.2:c.4932T>G	ENSP00000489431.2:p.Thr1644=
ENST00000644379.2:c.5121T>G	ENSP00000496570.2:p.Thr1707=
ENST00000644555.2:c.1605T>G	ENSP00000494614.2:p.Thr535=
ENST00000652672.2:c.4914T>G	ENSP00000498906.2:p.Thr1638=
ENST00000484087.6:c.1617T>G	ENSP00000419481.2:p.Thr539=
ENST00000357654.9:c.5055T>G MANE Select	ENSP00000350283.3:p.Thr1685=
ENST00000471181.7:c.5118T>G	ENSP00000418960.2:p.Thr1706=
ENST00000644379.1:c.1442T>G
ENST00000352993.7:c.1629T>G	ENSP00000312236.5:p.Thr543=
ENST00000357654.7:c.5055T>G	ENSP00000350283.3:p.Thr1685=
ENST00000461221.5:c.*4838T>G	ENSP00000418548.1:n.*4838T>G
ENST00000468300.5:c.1743T>G	ENSP00000417148.1:p.Thr581=
ENST00000471181.6:c.5118T>G	ENSP00000418960.2:p.Thr1706=
ENST00000472490.1:n.208T>G
ENST00000478531.5:c.1743T>G	ENSP00000420412.1:p.Thr581=
ENST00000484087.5:c.1368T>G	ENSP00000419481.1:p.Thr456=
ENST00000491747.6:c.1743T>G	ENSP00000420705.2:p.Thr581=
ENST00000493795.5:c.4914T>G	ENSP00000418775.1:p.Thr1638=
ENST00000493919.5:c.1605T>G	ENSP00000418819.1:p.Thr535=
ENST00000586385.5:c.5-3676T>G	ENSP00000465818.1:n.5-3676T>G
ENST00000591534.5:c.528T>G	ENSP00000467329.1:p.Thr176=
ENST00000591849.5:c.-98-17437T>G	ENSP00000465347.1:n.-98-17437T>G
NM_007294.3:c.5055T>G , LRG_292t1:c.5055T>G	NP_009225.1:p.Thr1685=
NM_007297.3:c.4914T>G	NP_009228.2:p.Thr1638=
NM_007298.3:c.1743T>G	NP_009229.2:p.Thr581=
NM_007299.3:c.1743T>G	NP_009230.2:p.Thr581=
NM_007300.3:c.5118T>G	NP_009231.2:p.Thr1706=
NR_027676.1:n.5191T>G
NM_007294.4:c.5055T>G MANE Select	NP_009225.1:p.Thr1685=
NM_007297.4:c.4914T>G	NP_009228.2:p.Thr1638=
NM_007299.4:c.1743T>G	NP_009230.2:p.Thr581=
NM_007300.4:c.5118T>G	NP_009231.2:p.Thr1706=
NR_027676.2:n.5232T>G