Canonical Allele Identifier: CA500148376

Gene: BRCA1

Linked Data

• dbSNP Id: rs2154150797
• MyVariant Identifiers: chr17:g.41234479T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43082462T>A , CM000679.2:g.43082462T>A	GRCh38
NC_000017.10:g.41234479T>A , CM000679.1:g.41234479T>A	GRCh37
NC_000017.9:g.38488005T>A	NCBI36
NG_005905.2:g.135522A>T , LRG_292:g.135522A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461574.2:c.4299A>T	ENSP00000417241.2:p.Ile1433=
ENST00000470026.6:c.4299A>T	ENSP00000419274.2:p.Ile1433=
ENST00000473961.6:c.4173A>T	ENSP00000420201.2:p.Ile1391=
ENST00000476777.6:c.4293A>T	ENSP00000417554.2:p.Ile1431=
ENST00000477152.6:c.4221A>T	ENSP00000419988.2:p.Ile1407=
ENST00000478531.6:c.987A>T	ENSP00000420412.2:p.Ile329=
ENST00000489037.2:c.4221A>T	ENSP00000420781.2:p.Ile1407=
ENST00000493919.6:c.849A>T	ENSP00000418819.2:p.Ile283=
ENST00000494123.6:c.4299A>T	ENSP00000419103.2:p.Ile1433=
ENST00000497488.2:c.3411A>T	ENSP00000418986.2:p.Ile1137=
ENST00000618469.2:c.4299A>T	ENSP00000478114.2:p.Ile1433=
ENST00000634433.2:c.4176A>T	ENSP00000489431.2:p.Ile1392=
ENST00000644379.2:c.4299A>T	ENSP00000496570.2:p.Ile1433=
ENST00000644555.2:c.849A>T	ENSP00000494614.2:p.Ile283=
ENST00000652672.2:c.4158A>T	ENSP00000498906.2:p.Ile1386=
ENST00000484087.6:c.864A>T	ENSP00000419481.2:p.Ile288=
ENST00000700182.1:c.909A>T	ENSP00000514849.1:p.Ile303=
ENST00000357654.9:c.4299A>T MANE Select	ENSP00000350283.3:p.Ile1433=
ENST00000471181.7:c.4299A>T	ENSP00000418960.2:p.Ile1433=
ENST00000644379.1:c.620A>T
ENST00000352993.7:c.873A>T	ENSP00000312236.5:p.Ile291=
ENST00000357654.7:c.4299A>T	ENSP00000350283.3:p.Ile1433=
ENST00000461221.5:c.*4082A>T	ENSP00000418548.1:n.*4082A>T
ENST00000461574.1:c.593A>T
ENST00000468300.5:c.990A>T	ENSP00000417148.1:p.Ile330=
ENST00000471181.6:c.4299A>T	ENSP00000418960.2:p.Ile1433=
ENST00000478531.5:c.987A>T	ENSP00000420412.1:p.Ile329=
ENST00000484087.5:c.612A>T	ENSP00000419481.1:p.Ile204=
ENST00000487825.5:c.615A>T	ENSP00000418212.1:p.Ile205=
ENST00000491747.6:c.990A>T	ENSP00000420705.2:p.Ile330=
ENST00000493795.5:c.4158A>T	ENSP00000418775.1:p.Ile1386=
ENST00000493919.5:c.849A>T	ENSP00000418819.1:p.Ile283=
ENST00000586385.5:c.5-18511A>T	ENSP00000465818.1:n.5-18511A>T
ENST00000591534.5:c.-43-7941A>T	ENSP00000467329.1:n.-43-7941A>T
ENST00000591849.5:c.-98-32272A>T	ENSP00000465347.1:n.-98-32272A>T
ENST00000621897.1:n.193A>T
NM_007294.3:c.4299A>T , LRG_292t1:c.4299A>T	NP_009225.1:p.Ile1433=
NM_007297.3:c.4158A>T	NP_009228.2:p.Ile1386=
NM_007298.3:c.990A>T	NP_009229.2:p.Ile330=
NM_007299.3:c.990A>T	NP_009230.2:p.Ile330=
NM_007300.3:c.4299A>T	NP_009231.2:p.Ile1433=
NR_027676.1:n.4435A>T
NM_007294.4:c.4299A>T MANE Select	NP_009225.1:p.Ile1433=
NM_007297.4:c.4158A>T	NP_009228.2:p.Ile1386=
NM_007299.4:c.990A>T	NP_009230.2:p.Ile330=
NM_007300.4:c.4299A>T	NP_009231.2:p.Ile1433=
NR_027676.2:n.4476A>T