Canonical Allele Identifier: CA2499306739
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43045669_43045682del , CM000679.2:g.43045669_43045682del GRCh38
NC_000017.10:g.41197686_41197699del , CM000679.1:g.41197686_41197699del GRCh37
NC_000017.9:g.38451212_38451225del NCBI36
NG_005905.2:g.172302_172315del , LRG_292:g.172302_172315del

Transcript Alleles

HGVS Amino-acid change
ENST00000461574.2:c.5585_*9del ENSP00000417241.2:n.[c.5585_*9del;Tyr1862...
ENST00000470026.6:c.5588_*9del ENSP00000419274.2:n.[c.5588_*9del;Tyr1863...
ENST00000473961.6:c.5462_*9del ENSP00000420201.2:n.[c.5462_*9del;Tyr1821...
ENST00000476777.6:c.5582_*9del ENSP00000417554.2:n.[c.5582_*9del;Tyr1861...
ENST00000477152.6:c.5510_*9del ENSP00000419988.2:n.[c.5510_*9del;Tyr1837...
ENST00000478531.6:c.2276_*9del ENSP00000420412.2:n.[c.2276_*9del;Tyr759C...
ENST00000489037.2:c.5510_*9del ENSP00000420781.2:n.[c.5510_*9del;Tyr1837...
ENST00000493919.6:c.2138_*9del ENSP00000418819.2:n.[c.2138_*9del;Tyr713C...
ENST00000494123.6:c.5588_*9del ENSP00000419103.2:n.[c.5588_*9del;Tyr1863...
ENST00000497488.2:c.4700_*9del ENSP00000418986.2:n.[c.4700_*9del;Tyr1567...
ENST00000618469.2:c.5588_*9del ENSP00000478114.2:n.[c.5588_*9del;Tyr1863...
ENST00000634433.2:c.5465_*9del ENSP00000489431.2:n.[c.5465_*9del;Tyr1822...
ENST00000644379.2:c.5654_*9del ENSP00000496570.2:n.[c.5654_*9del;Tyr1885...
ENST00000644555.2:c.2138_*9del ENSP00000494614.2:n.[c.2138_*9del;Tyr713C...
ENST00000652672.2:c.5447_*9del ENSP00000498906.2:n.[c.5447_*9del;Tyr1816...
ENST00000484087.6:c.2150_*9del ENSP00000419481.2:n.[c.2150_*9del;Tyr717C...
ENST00000700081.1:n.1471_1484del
ENST00000700082.1:n.952_965del
ENST00000357654.9:c.5588_*9del MANE Select ENSP00000350283.3:n.[c.5588_*9del;Tyr1863...
ENST00000471181.7:c.5651_*9del ENSP00000418960.2:n.[c.5651_*9del;Tyr1884...
ENST00000644379.1:c.1975_1988del
ENST00000352993.7:c.2162_*9del ENSP00000312236.5:n.[c.2162_*9del;Tyr721C...
ENST00000357654.7:c.5588_*9del ENSP00000350283.3:n.[c.5588_*9del;Tyr1863...
ENST00000468300.5:c.*102_*115del ENSP00000417148.1:n.*102_*115del
ENST00000471181.6:c.5651_*9del ENSP00000418960.2:n.[c.5651_*9del;Tyr1884...
ENST00000493795.5:c.5447_*9del ENSP00000418775.1:n.[c.5447_*9del;Tyr1816...
ENST00000586385.5:c.518_*9del ENSP00000465818.1:n.[c.518_*9del;Tyr173Cy...
ENST00000591534.5:c.1061_*9del ENSP00000467329.1:n.[c.1061_*9del;Tyr354C...
ENST00000591849.5:c.287_*9del ENSP00000465347.1:n.[c.287_*9del;Tyr96Cys...
NM_007294.3:c.5588_*9del , LRG_292t1:c.5588_*9del NP_009225.1:n.[c.5588_*9del;Tyr1863CysfsT...
NM_007297.3:c.5447_*9del NP_009228.2:n.[c.5447_*9del;Tyr1816CysfsT...
NM_007298.3:c.2276_*9del NP_009229.2:n.[c.2276_*9del;Tyr759CysfsTe...
NM_007299.3:c.*102_*115del NP_009230.2:n.*102_*115del
NM_007300.3:c.5651_*9del NP_009231.2:n.[c.5651_*9del;Tyr1884CysfsT...
NR_027676.1:n.5724_5737del
NM_007294.4:c.5588_*9del MANE Select NP_009225.1:n.[c.5588_*9del;Tyr1863CysfsT...
NM_007297.4:c.5447_*9del NP_009228.2:n.[c.5447_*9del;Tyr1816CysfsT...
NM_007299.4:c.*102_*115del NP_009230.2:n.*102_*115del
NM_007300.4:c.5651_*9del NP_009231.2:n.[c.5651_*9del;Tyr1884CysfsT...
NR_027676.2:n.5765_5778del