Canonical Allele Identifier: CA2260775472
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43076525T= , CM000679.2:g.43076525T= GRCh38
NC_000017.10:g.41228542T= , CM000679.1:g.41228542T= GRCh37
NC_000017.9:g.38482068T= NCBI36
NG_005905.2:g.141459A= , LRG_292:g.141459A=

Transcript Alleles

HGVS Amino-acid change
ENST00000461574.2:c.4444A= ENSP00000417241.2:p.Ser1482=
ENST00000470026.6:c.4447A= ENSP00000419274.2:p.Ser1483=
ENST00000473961.6:c.4321A= ENSP00000420201.2:p.Ser1441=
ENST00000476777.6:c.4441A= ENSP00000417554.2:p.Ser1481=
ENST00000477152.6:c.4369A= ENSP00000419988.2:p.Ser1457=
ENST00000478531.6:c.1135A= ENSP00000420412.2:p.Ser379=
ENST00000489037.2:c.4369A= ENSP00000420781.2:p.Ser1457=
ENST00000493919.6:c.997A= ENSP00000418819.2:p.Ser333=
ENST00000494123.6:c.4447A= ENSP00000419103.2:p.Ser1483=
ENST00000497488.2:c.3559A= ENSP00000418986.2:p.Ser1187=
ENST00000618469.2:c.4447A= ENSP00000478114.2:p.Ser1483=
ENST00000634433.2:c.4324A= ENSP00000489431.2:p.Ser1442=
ENST00000644379.2:c.4513A= ENSP00000496570.2:p.Ser1505=
ENST00000644555.2:c.997A= ENSP00000494614.2:p.Ser333=
ENST00000652672.2:c.4306A= ENSP00000498906.2:p.Ser1436=
ENST00000484087.6:c.1009A= ENSP00000419481.2:p.Ser337=
ENST00000700182.1:c.1054A= ENSP00000514849.1:p.Ser352=
ENST00000357654.9:c.4447A= MANE Select ENSP00000350283.3:p.Ser1483=
ENST00000471181.7:c.4510A= ENSP00000418960.2:p.Ser1504=
ENST00000644379.1:c.834A=
ENST00000352993.7:c.1021A= ENSP00000312236.5:p.Ser341=
ENST00000357654.7:c.4447A= ENSP00000350283.3:p.Ser1483=
ENST00000461221.5:c.*4230A= ENSP00000418548.1:n.*4230A=
ENST00000468300.5:c.1135A= ENSP00000417148.1:p.Ser379=
ENST00000471181.6:c.4510A= ENSP00000418960.2:p.Ser1504=
ENST00000478531.5:c.1135A= ENSP00000420412.1:p.Ser379=
ENST00000484087.5:c.760A= ENSP00000419481.1:p.Ser254=
ENST00000487825.5:c.763A= ENSP00000418212.1:p.Ser255=
ENST00000491747.6:c.1135A= ENSP00000420705.2:p.Ser379=
ENST00000493795.5:c.4306A= ENSP00000418775.1:p.Ser1436=
ENST00000493919.5:c.997A= ENSP00000418819.1:p.Ser333=
ENST00000586385.5:c.5-12574A= ENSP00000465818.1:n.5-12574A=
ENST00000591534.5:c.-43-2004A= ENSP00000467329.1:n.-43-2004A=
ENST00000591849.5:c.-98-26335A= ENSP00000465347.1:n.-98-26335A=
ENST00000621897.1:n.338A=
NM_007294.3:c.4447A= , LRG_292t1:c.4447A= NP_009225.1:p.Ser1483=
NM_007297.3:c.4306A= NP_009228.2:p.Ser1436=
NM_007298.3:c.1135A= NP_009229.2:p.Ser379=
NM_007299.3:c.1135A= NP_009230.2:p.Ser379=
NM_007300.3:c.4510A= NP_009231.2:p.Ser1504=
NR_027676.1:n.4583A=
NM_007294.4:c.4447A= MANE Select NP_009225.1:p.Ser1483=
NM_007297.4:c.4306A= NP_009228.2:p.Ser1436=
NM_007299.4:c.1135A= NP_009230.2:p.Ser379=
NM_007300.4:c.4510A= NP_009231.2:p.Ser1504=
NR_027676.2:n.4624A=