Canonical Allele Identifier: CA001596
Gene: BRCA1 HGNC NCBI

Linked Data

dbSNP Id: rs80357706

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43093129_43093130del , CM000679.2:g.43093129_43093130del GRCh38
NC_000017.10:g.41245146_41245147del , CM000679.1:g.41245146_41245147del GRCh37
NC_000017.9:g.38498672_38498673del NCBI36
NG_005905.2:g.124858_124859del , LRG_292:g.124858_124859del

Transcript Alleles

HGVS Amino-acid change
ENST00000354071.8:n.2469_2470del
ENST00000461574.2:c.2405_2406del ENSP00000417241.2:p.Val802GlufsTer7
ENST00000470026.6:c.2405_2406del ENSP00000419274.2:p.Val802GlufsTer7
ENST00000473961.6:c.2279_2280del ENSP00000420201.2:p.Val760GlufsTer7
ENST00000476777.6:c.2402_2403del ENSP00000417554.2:p.Val801GlufsTer7
ENST00000477152.6:c.2327_2328del ENSP00000419988.2:p.Val776GlufsTer7
ENST00000478531.6:c.784+1618_784+1619del ENSP00000420412.2:n.784+1618_784+1619del
ENST00000489037.2:c.2327_2328del ENSP00000420781.2:p.Val776GlufsTer7
ENST00000493919.6:c.646+1618_646+1619del ENSP00000418819.2:n.646+1618_646+1619del
ENST00000494123.6:c.2405_2406del ENSP00000419103.2:p.Val802GlufsTer7
ENST00000497488.2:c.1517_1518del ENSP00000418986.2:p.Val506GlufsTer7
ENST00000618469.2:c.2405_2406del ENSP00000478114.2:p.Val802GlufsTer7
ENST00000634433.2:c.2282_2283del ENSP00000489431.2:p.Val761GlufsTer7
ENST00000644379.2:c.2405_2406del ENSP00000496570.2:p.Val802GlufsTer7
ENST00000644555.2:c.646+1618_646+1619del ENSP00000494614.2:n.646+1618_646+1619del
ENST00000652672.2:c.2264_2265del ENSP00000498906.2:p.Val755GlufsTer7
ENST00000484087.6:c.664+1618_664+1619del ENSP00000419481.2:n.664+1618_664+1619del
ENST00000700182.1:c.706+1618_706+1619del ENSP00000514849.1:n.706+1618_706+1619del
ENST00000357654.9:c.2405_2406del MANE Select ENSP00000350283.3:p.Val802GlufsTer7
ENST00000471181.7:c.2405_2406del ENSP00000418960.2:p.Val802GlufsTer7
ENST00000352993.7:c.671-2094_671-2093del ENSP00000312236.5:n.671-2094_671-2093del
ENST00000354071.7:c.2405_2406del ENSP00000326002.7:p.Val802GlufsTer7
ENST00000357654.7:c.2405_2406del ENSP00000350283.3:p.Val802GlufsTer7
ENST00000461221.5:c.*2188_*2189del ENSP00000418548.1:n.*2188_*2189del
ENST00000468300.5:c.787+1618_787+1619del ENSP00000417148.1:n.787+1618_787+1619del
ENST00000471181.6:c.2405_2406del ENSP00000418960.2:p.Val802GlufsTer7
ENST00000478531.5:c.784+1618_784+1619del ENSP00000420412.1:n.784+1618_784+1619del
ENST00000484087.5:c.409+1618_409+1619del ENSP00000419481.1:n.409+1618_409+1619del
ENST00000487825.5:c.412+1618_412+1619del ENSP00000418212.1:n.412+1618_412+1619del
ENST00000491747.6:c.787+1618_787+1619del ENSP00000420705.2:n.787+1618_787+1619del
ENST00000493795.5:c.2264_2265del ENSP00000418775.1:p.Val755GlufsTer7
ENST00000493919.5:c.646+1618_646+1619del ENSP00000418819.1:n.646+1618_646+1619del
ENST00000586385.5:c.5-29175_5-29174del ENSP00000465818.1:n.5-29175_5-29174del
ENST00000591534.5:c.-43-18605_-43-18604del ENSP00000467329.1:n.-43-18605_-43-18604de...
ENST00000591849.5:c.-99+32145_-99+32146del ENSP00000465347.1:n.-99+32145_-99+32146de...
ENST00000634433.1:c.2282_2283del ENSP00000489431.1:p.Val761GlufsTer7
NM_007294.3:c.2405_2406del , LRG_292t1:c.2405_2406del NP_009225.1:p.Val802GlufsTer7
NM_007297.3:c.2264_2265del NP_009228.2:p.Val755GlufsTer7
NM_007298.3:c.787+1618_787+1619del NP_009229.2:n.787+1618_787+1619del
NM_007299.3:c.787+1618_787+1619del NP_009230.2:n.787+1618_787+1619del
NM_007300.3:c.2405_2406del NP_009231.2:p.Val802GlufsTer7
NR_027676.1:n.2541_2542del
NM_007294.4:c.2405_2406del MANE Select NP_009225.1:p.Val802GlufsTer7
NM_007297.4:c.2264_2265del NP_009228.2:p.Val755GlufsTer7
NM_007299.4:c.787+1618_787+1619del NP_009230.2:n.787+1618_787+1619del
NM_007300.4:c.2405_2406del NP_009231.2:p.Val802GlufsTer7
NR_027676.2:n.2582_2583del