Canonical Allele Identifier: CA001738

Gene: BRCA1

Linked Data - Expert Curation

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43092876_43092877del , CM000679.2:g.43092876_43092877del	GRCh38
NC_000017.10:g.41244893_41244894del , CM000679.1:g.41244893_41244894del	GRCh37
NC_000017.9:g.38498419_38498420del	NCBI36
NG_005905.2:g.125110_125111del , LRG_292:g.125110_125111del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354071.8:n.2721_2722del
ENST00000461574.2:c.2657_2658del	ENSP00000417241.2:p.Ser886CysfsTer16
ENST00000470026.6:c.2657_2658del	ENSP00000419274.2:p.Ser886CysfsTer16
ENST00000473961.6:c.2531_2532del	ENSP00000420201.2:p.Ser844CysfsTer16
ENST00000476777.6:c.2654_2655del	ENSP00000417554.2:p.Ser885CysfsTer16
ENST00000477152.6:c.2579_2580del	ENSP00000419988.2:p.Ser860CysfsTer16
ENST00000478531.6:c.785-1842_785-1841del	ENSP00000420412.2:n.785-1842_785-1841del
ENST00000489037.2:c.2579_2580del	ENSP00000420781.2:p.Ser860CysfsTer16
ENST00000493919.6:c.647-1842_647-1841del	ENSP00000418819.2:n.647-1842_647-1841del
ENST00000494123.6:c.2657_2658del	ENSP00000419103.2:p.Ser886CysfsTer16
ENST00000497488.2:c.1769_1770del	ENSP00000418986.2:p.Ser590CysfsTer16
ENST00000618469.2:c.2657_2658del	ENSP00000478114.2:p.Ser886CysfsTer16
ENST00000634433.2:c.2534_2535del	ENSP00000489431.2:p.Ser845CysfsTer16
ENST00000644379.2:c.2657_2658del	ENSP00000496570.2:p.Ser886CysfsTer16
ENST00000644555.2:c.647-1842_647-1841del	ENSP00000494614.2:n.647-1842_647-1841del
ENST00000652672.2:c.2516_2517del	ENSP00000498906.2:p.Ser839CysfsTer16
ENST00000484087.6:c.665-1842_665-1841del	ENSP00000419481.2:n.665-1842_665-1841del
ENST00000700182.1:c.707-1842_707-1841del	ENSP00000514849.1:n.707-1842_707-1841del
ENST00000357654.9:c.2657_2658del MANE Select	ENSP00000350283.3:p.Ser886CysfsTer16
ENST00000471181.7:c.2657_2658del	ENSP00000418960.2:p.Ser886CysfsTer16
ENST00000352993.7:c.671-1842_671-1841del	ENSP00000312236.5:n.671-1842_671-1841del
ENST00000354071.7:c.2657_2658del	ENSP00000326002.7:p.Ser886CysfsTer16
ENST00000357654.7:c.2657_2658del	ENSP00000350283.3:p.Ser886CysfsTer16
ENST00000461221.5:c.*2440_*2441del	ENSP00000418548.1:n.*2440_*2441del
ENST00000468300.5:c.788-1842_788-1841del	ENSP00000417148.1:n.788-1842_788-1841del
ENST00000471181.6:c.2657_2658del	ENSP00000418960.2:p.Ser886CysfsTer16
ENST00000478531.5:c.785-1842_785-1841del	ENSP00000420412.1:n.785-1842_785-1841del
ENST00000484087.5:c.410-1842_410-1841del	ENSP00000419481.1:n.410-1842_410-1841del
ENST00000487825.5:c.413-1842_413-1841del	ENSP00000418212.1:n.413-1842_413-1841del
ENST00000491747.6:c.788-1842_788-1841del	ENSP00000420705.2:n.788-1842_788-1841del
ENST00000493795.5:c.2516_2517del	ENSP00000418775.1:p.Ser839CysfsTer16
ENST00000493919.5:c.647-1842_647-1841del	ENSP00000418819.1:n.647-1842_647-1841del
ENST00000586385.5:c.5-28923_5-28922del	ENSP00000465818.1:n.5-28923_5-28922del
ENST00000591534.5:c.-43-18353_-43-18352del	ENSP00000467329.1:n.-43-18353_-43-18352del
ENST00000591849.5:c.-99+32397_-99+32398del	ENSP00000465347.1:n.-99+32397_-99+32398del
NM_007294.3:c.2657_2658del , LRG_292t1:c.2657_2658del	NP_009225.1:p.Ser886CysfsTer16
NM_007297.3:c.2516_2517del	NP_009228.2:p.Ser839CysfsTer16
NM_007298.3:c.788-1842_788-1841del	NP_009229.2:n.788-1842_788-1841del
NM_007299.3:c.788-1842_788-1841del	NP_009230.2:n.788-1842_788-1841del
NM_007300.3:c.2657_2658del	NP_009231.2:p.Ser886CysfsTer16
NR_027676.1:n.2793_2794del
NM_007294.4:c.2657_2658del MANE Select	NP_009225.1:p.Ser886CysfsTer16
NM_007297.4:c.2516_2517del	NP_009228.2:p.Ser839CysfsTer16
NM_007299.4:c.788-1842_788-1841del	NP_009230.2:n.788-1842_788-1841del
NM_007300.4:c.2657_2658del	NP_009231.2:p.Ser886CysfsTer16
NR_027676.2:n.2834_2835del