Canonical Allele Identifier: CA003256

Gene: BRCA1

Linked Data

• ClinVar Variation Id: 55409
• ClinVar RCV Id: RCV000256527
• dbSNP Id: rs397509229
• MyVariant Identifiers: chr17:g.41215915C>A (hg19) ; chr17:g.43063898C>A (hg38)
• PubMed: PMID:11084537

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43063898C>A , CM000679.2:g.43063898C>A	GRCh38
NC_000017.10:g.41215915C>A , CM000679.1:g.41215915C>A	GRCh37
NC_000017.9:g.38469441C>A	NCBI36
NG_005905.2:g.154086G>T , LRG_292:g.154086G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461574.2:c.5125G>T	ENSP00000417241.2:p.Gly1709Ter
ENST00000470026.6:c.5128G>T	ENSP00000419274.2:p.Gly1710Ter
ENST00000473961.6:c.5002G>T	ENSP00000420201.2:p.Gly1668Ter
ENST00000476777.6:c.5122G>T	ENSP00000417554.2:p.Gly1708Ter
ENST00000477152.6:c.5050G>T	ENSP00000419988.2:p.Gly1684Ter
ENST00000478531.6:c.1816G>T	ENSP00000420412.2:p.Gly606Ter
ENST00000489037.2:c.5050G>T	ENSP00000420781.2:p.Gly1684Ter
ENST00000493919.6:c.1678G>T	ENSP00000418819.2:p.Gly560Ter
ENST00000494123.6:c.5128G>T	ENSP00000419103.2:p.Gly1710Ter
ENST00000497488.2:c.4240G>T	ENSP00000418986.2:p.Gly1414Ter
ENST00000618469.2:c.5128G>T	ENSP00000478114.2:p.Gly1710Ter
ENST00000634433.2:c.5005G>T	ENSP00000489431.2:p.Gly1669Ter
ENST00000644379.2:c.5194G>T	ENSP00000496570.2:p.Gly1732Ter
ENST00000644555.2:c.1678G>T	ENSP00000494614.2:p.Gly560Ter
ENST00000652672.2:c.4987G>T	ENSP00000498906.2:p.Gly1663Ter
ENST00000484087.6:c.1690G>T	ENSP00000419481.2:p.Gly564Ter
ENST00000357654.9:c.5128G>T MANE Select	ENSP00000350283.3:p.Gly1710Ter
ENST00000471181.7:c.5191G>T	ENSP00000418960.2:p.Gly1731Ter
ENST00000644379.1:c.1515G>T
ENST00000352993.7:c.1702G>T	ENSP00000312236.5:p.Gly568Ter
ENST00000357654.7:c.5128G>T	ENSP00000350283.3:p.Gly1710Ter
ENST00000461221.5:c.*4911G>T	ENSP00000418548.1:n.*4911G>T
ENST00000468300.5:c.1816G>T	ENSP00000417148.1:p.Gly606Ter
ENST00000471181.6:c.5191G>T	ENSP00000418960.2:p.Gly1731Ter
ENST00000478531.5:c.1816G>T	ENSP00000420412.1:p.Gly606Ter
ENST00000484087.5:c.1441G>T	ENSP00000419481.1:p.Gly481Ter
ENST00000491747.6:c.1816G>T	ENSP00000420705.2:p.Gly606Ter
ENST00000493795.5:c.4987G>T	ENSP00000418775.1:p.Gly1663Ter
ENST00000493919.5:c.1678G>T	ENSP00000418819.1:p.Gly560Ter
ENST00000586385.5:c.58G>T	ENSP00000465818.1:p.Gly20Ter
ENST00000591534.5:c.601G>T	ENSP00000467329.1:p.Gly201Ter
ENST00000591849.5:c.-98-13708G>T	ENSP00000465347.1:n.-98-13708G>T
NM_007294.3:c.5128G>T , LRG_292t1:c.5128G>T	NP_009225.1:p.Gly1710Ter
NM_007297.3:c.4987G>T	NP_009228.2:p.Gly1663Ter
NM_007298.3:c.1816G>T	NP_009229.2:p.Gly606Ter
NM_007299.3:c.1816G>T	NP_009230.2:p.Gly606Ter
NM_007300.3:c.5191G>T	NP_009231.2:p.Gly1731Ter
NR_027676.1:n.5264G>T
NM_007294.4:c.5128G>T MANE Select	NP_009225.1:p.Gly1710Ter
NM_007297.4:c.4987G>T	NP_009228.2:p.Gly1663Ter
NM_007299.4:c.1816G>T	NP_009230.2:p.Gly606Ter
NM_007300.4:c.5191G>T	NP_009231.2:p.Gly1731Ter
NR_027676.2:n.5305G>T