Canonical Allele Identifier: CA10593286

Gene: BRCA1

Linked Data

• MyVariant Identifiers: chr17:g.41234561T>A (hg19) ; chr17:g.43082544T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43082544T>A , CM000679.2:g.43082544T>A	GRCh38
NC_000017.10:g.41234561T>A , CM000679.1:g.41234561T>A	GRCh37
NC_000017.9:g.38488087T>A	NCBI36
NG_005905.2:g.135440A>T , LRG_292:g.135440A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461574.2:c.4217A>T	ENSP00000417241.2:p.Lys1406Met
ENST00000470026.6:c.4217A>T	ENSP00000419274.2:p.Lys1406Met
ENST00000473961.6:c.4091A>T	ENSP00000420201.2:p.Lys1364Met
ENST00000476777.6:c.4211A>T	ENSP00000417554.2:p.Lys1404Met
ENST00000477152.6:c.4139A>T	ENSP00000419988.2:p.Lys1380Met
ENST00000478531.6:c.905A>T	ENSP00000420412.2:p.Lys302Met
ENST00000489037.2:c.4139A>T	ENSP00000420781.2:p.Lys1380Met
ENST00000493919.6:c.767A>T	ENSP00000418819.2:p.Lys256Met
ENST00000494123.6:c.4217A>T	ENSP00000419103.2:p.Lys1406Met
ENST00000497488.2:c.3329A>T	ENSP00000418986.2:p.Lys1110Met
ENST00000618469.2:c.4217A>T	ENSP00000478114.2:p.Lys1406Met
ENST00000634433.2:c.4094A>T	ENSP00000489431.2:p.Lys1365Met
ENST00000644379.2:c.4217A>T	ENSP00000496570.2:p.Lys1406Met
ENST00000644555.2:c.767A>T	ENSP00000494614.2:p.Lys256Met
ENST00000652672.2:c.4076A>T	ENSP00000498906.2:p.Lys1359Met
ENST00000484087.6:c.782A>T	ENSP00000419481.2:p.Lys261Met
ENST00000700182.1:c.827A>T	ENSP00000514849.1:p.Lys276Met
ENST00000357654.9:c.4217A>T MANE Select	ENSP00000350283.3:p.Lys1406Met
ENST00000471181.7:c.4217A>T	ENSP00000418960.2:p.Lys1406Met
ENST00000644379.1:c.538A>T
ENST00000352993.7:c.791A>T	ENSP00000312236.5:p.Lys264Met
ENST00000357654.7:c.4217A>T	ENSP00000350283.3:p.Lys1406Met
ENST00000461221.5:c.*4000A>T	ENSP00000418548.1:n.*4000A>T
ENST00000461574.1:c.511A>T
ENST00000468300.5:c.908A>T	ENSP00000417148.1:p.Lys303Met
ENST00000471181.6:c.4217A>T	ENSP00000418960.2:p.Lys1406Met
ENST00000478531.5:c.905A>T	ENSP00000420412.1:p.Lys302Met
ENST00000484087.5:c.530A>T	ENSP00000419481.1:p.Lys177Met
ENST00000487825.5:c.533A>T	ENSP00000418212.1:p.Lys178Met
ENST00000491747.6:c.908A>T	ENSP00000420705.2:p.Lys303Met
ENST00000493795.5:c.4076A>T	ENSP00000418775.1:p.Lys1359Met
ENST00000493919.5:c.767A>T	ENSP00000418819.1:p.Lys256Met
ENST00000586385.5:c.5-18593A>T	ENSP00000465818.1:n.5-18593A>T
ENST00000591534.5:c.-43-8023A>T	ENSP00000467329.1:n.-43-8023A>T
ENST00000591849.5:c.-98-32354A>T	ENSP00000465347.1:n.-98-32354A>T
ENST00000621897.1:n.111A>T
NM_007294.3:c.4217A>T , LRG_292t1:c.4217A>T	NP_009225.1:p.Lys1406Met
NM_007297.3:c.4076A>T	NP_009228.2:p.Lys1359Met
NM_007298.3:c.908A>T	NP_009229.2:p.Lys303Met
NM_007299.3:c.908A>T	NP_009230.2:p.Lys303Met
NM_007300.3:c.4217A>T	NP_009231.2:p.Lys1406Met
NR_027676.1:n.4353A>T
NM_007294.4:c.4217A>T MANE Select	NP_009225.1:p.Lys1406Met
NM_007297.4:c.4076A>T	NP_009228.2:p.Lys1359Met
NM_007299.4:c.908A>T	NP_009230.2:p.Lys303Met
NM_007300.4:c.4217A>T	NP_009231.2:p.Lys1406Met
NR_027676.2:n.4394A>T