Canonical Allele Identifier: CA10580507

Gene: BRCA1

Linked Data

• ClinVar Variation Id: 231443
• ClinVar RCV Id: RCV000219146 ; RCV001209529 ; RCV003316216
• dbSNP Id: rs876659163
• MyVariant Identifiers: chr17:g.41223075G>A (hg19) ; chr17:g.43071058G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43071058G>A , CM000679.2:g.43071058G>A	GRCh38
NC_000017.10:g.41223075G>A , CM000679.1:g.41223075G>A	GRCh37
NC_000017.9:g.38476601G>A	NCBI36
NG_005905.2:g.146926C>T , LRG_292:g.146926C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461574.2:c.4853C>T	ENSP00000417241.2:p.Thr1618Ile
ENST00000470026.6:c.4856C>T	ENSP00000419274.2:p.Thr1619Ile
ENST00000473961.6:c.4730C>T	ENSP00000420201.2:p.Thr1577Ile
ENST00000476777.6:c.4850C>T	ENSP00000417554.2:p.Thr1617Ile
ENST00000477152.6:c.4778C>T	ENSP00000419988.2:p.Thr1593Ile
ENST00000478531.6:c.1544C>T	ENSP00000420412.2:p.Thr515Ile
ENST00000489037.2:c.4778C>T	ENSP00000420781.2:p.Thr1593Ile
ENST00000493919.6:c.1406C>T	ENSP00000418819.2:p.Thr469Ile
ENST00000494123.6:c.4856C>T	ENSP00000419103.2:p.Thr1619Ile
ENST00000497488.2:c.3968C>T	ENSP00000418986.2:p.Thr1323Ile
ENST00000618469.2:c.4856C>T	ENSP00000478114.2:p.Thr1619Ile
ENST00000634433.2:c.4733C>T	ENSP00000489431.2:p.Thr1578Ile
ENST00000644379.2:c.4922C>T	ENSP00000496570.2:p.Thr1641Ile
ENST00000644555.2:c.1406C>T	ENSP00000494614.2:p.Thr469Ile
ENST00000652672.2:c.4715C>T	ENSP00000498906.2:p.Thr1572Ile
ENST00000484087.6:c.1418C>T	ENSP00000419481.2:p.Thr473Ile
ENST00000700182.1:c.1463C>T	ENSP00000514849.1:p.Thr488Ile
ENST00000357654.9:c.4856C>T MANE Select	ENSP00000350283.3:p.Thr1619Ile
ENST00000471181.7:c.4919C>T	ENSP00000418960.2:p.Thr1640Ile
ENST00000644379.1:c.1243C>T
ENST00000352993.7:c.1430C>T	ENSP00000312236.5:p.Thr477Ile
ENST00000357654.7:c.4856C>T	ENSP00000350283.3:p.Thr1619Ile
ENST00000461221.5:c.*4639C>T	ENSP00000418548.1:n.*4639C>T
ENST00000468300.5:c.1544C>T	ENSP00000417148.1:p.Thr515Ile
ENST00000471181.6:c.4919C>T	ENSP00000418960.2:p.Thr1640Ile
ENST00000472490.1:n.9C>T
ENST00000478531.5:c.1544C>T	ENSP00000420412.1:p.Thr515Ile
ENST00000484087.5:c.1169C>T	ENSP00000419481.1:p.Thr390Ile
ENST00000491747.6:c.1544C>T	ENSP00000420705.2:p.Thr515Ile
ENST00000493795.5:c.4715C>T	ENSP00000418775.1:p.Thr1572Ile
ENST00000493919.5:c.1406C>T	ENSP00000418819.1:p.Thr469Ile
ENST00000586385.5:c.5-7107C>T	ENSP00000465818.1:n.5-7107C>T
ENST00000591534.5:c.329C>T	ENSP00000467329.1:p.Thr110Ile
ENST00000591849.5:c.-98-20868C>T	ENSP00000465347.1:n.-98-20868C>T
NM_007294.3:c.4856C>T , LRG_292t1:c.4856C>T	NP_009225.1:p.Thr1619Ile
NM_007297.3:c.4715C>T	NP_009228.2:p.Thr1572Ile
NM_007298.3:c.1544C>T	NP_009229.2:p.Thr515Ile
NM_007299.3:c.1544C>T	NP_009230.2:p.Thr515Ile
NM_007300.3:c.4919C>T	NP_009231.2:p.Thr1640Ile
NR_027676.1:n.4992C>T
NM_007294.4:c.4856C>T MANE Select	NP_009225.1:p.Thr1619Ile
NM_007297.4:c.4715C>T	NP_009228.2:p.Thr1572Ile
NM_007299.4:c.1544C>T	NP_009230.2:p.Thr515Ile
NM_007300.4:c.4919C>T	NP_009231.2:p.Thr1640Ile
NR_027676.2:n.5033C>T