Canonical Allele Identifier: CA2260783333

Gene: BRCA1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43092694_43092697delinsATAC , CM000679.2:g.43092694_43092697delinsATAC	GRCh38
NC_000017.10:g.41244711_41244714delinsATAC , CM000679.1:g.41244711_41244714delinsATAC	GRCh37
NC_000017.9:g.38498237_38498240delinsATAC	NCBI36
NG_005905.2:g.125287_125290delinsGTAT , LRG_292:g.125287_125290delinsGTAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000354071.8:n.2898_2901delinsGTAT
ENST00000461574.2:c.2834_2837delinsGTAT	ENSP00000417241.2:p.Ser945=
ENST00000470026.6:c.2834_2837delinsGTAT	ENSP00000419274.2:p.Ser945=
ENST00000473961.6:c.2708_2711delinsGTAT	ENSP00000420201.2:p.Ser903=
ENST00000476777.6:c.2831_2834delinsGTAT	ENSP00000417554.2:p.Ser944=
ENST00000477152.6:c.2756_2759delinsGTAT	ENSP00000419988.2:p.Ser919=
ENST00000478531.6:c.785-1665_785-1662delinsGTAT	ENSP00000420412.2:n.785-1665_785-1662delinsGTAT
ENST00000489037.2:c.2756_2759delinsGTAT	ENSP00000420781.2:p.Ser919=
ENST00000493919.6:c.647-1665_647-1662delinsGTAT	ENSP00000418819.2:n.647-1665_647-1662delinsGTAT
ENST00000494123.6:c.2834_2837delinsGTAT	ENSP00000419103.2:p.Ser945=
ENST00000497488.2:c.1946_1949delinsGTAT	ENSP00000418986.2:p.Ser649=
ENST00000618469.2:c.2834_2837delinsGTAT	ENSP00000478114.2:p.Ser945=
ENST00000634433.2:c.2711_2714delinsGTAT	ENSP00000489431.2:p.Ser904=
ENST00000644379.2:c.2834_2837delinsGTAT	ENSP00000496570.2:p.Ser945=
ENST00000644555.2:c.647-1665_647-1662delinsGTAT	ENSP00000494614.2:n.647-1665_647-1662delinsGTAT
ENST00000652672.2:c.2693_2696delinsGTAT	ENSP00000498906.2:p.Ser898=
ENST00000484087.6:c.665-1665_665-1662delinsGTAT	ENSP00000419481.2:n.665-1665_665-1662delinsGTAT
ENST00000700182.1:c.707-1665_707-1662delinsGTAT	ENSP00000514849.1:n.707-1665_707-1662delinsGTAT
ENST00000357654.9:c.2834_2837delinsGTAT MANE Select	ENSP00000350283.3:p.Ser945=
ENST00000471181.7:c.2834_2837delinsGTAT	ENSP00000418960.2:p.Ser945=
ENST00000352993.7:c.671-1665_671-1662delinsGTAT	ENSP00000312236.5:n.671-1665_671-1662delinsGTAT
ENST00000354071.7:c.2834_2837delinsGTAT	ENSP00000326002.7:p.Ser945=
ENST00000357654.7:c.2834_2837delinsGTAT	ENSP00000350283.3:p.Ser945=
ENST00000461221.5:c.*2617_*2620delinsGTAT	ENSP00000418548.1:n.*2617_*2620delinsGTAT
ENST00000468300.5:c.788-1665_788-1662delinsGTAT	ENSP00000417148.1:n.788-1665_788-1662delinsGTAT
ENST00000471181.6:c.2834_2837delinsGTAT	ENSP00000418960.2:p.Ser945=
ENST00000478531.5:c.785-1665_785-1662delinsGTAT	ENSP00000420412.1:n.785-1665_785-1662delinsGTAT
ENST00000484087.5:c.410-1665_410-1662delinsGTAT	ENSP00000419481.1:n.410-1665_410-1662delinsGTAT
ENST00000487825.5:c.413-1665_413-1662delinsGTAT	ENSP00000418212.1:n.413-1665_413-1662delinsGTAT
ENST00000491747.6:c.788-1665_788-1662delinsGTAT	ENSP00000420705.2:n.788-1665_788-1662delinsGTAT
ENST00000493795.5:c.2693_2696delinsGTAT	ENSP00000418775.1:p.Ser898=
ENST00000493919.5:c.647-1665_647-1662delinsGTAT	ENSP00000418819.1:n.647-1665_647-1662delinsGTAT
ENST00000586385.5:c.5-28746_5-28743delinsGTAT	ENSP00000465818.1:n.5-28746_5-28743delinsGTAT
ENST00000591534.5:c.-43-18176_-43-18173delinsGTAT	ENSP00000467329.1:n.-43-18176_-43-18173delinsGTAT
ENST00000591849.5:c.-99+32574_-99+32577delinsGTAT	ENSP00000465347.1:n.-99+32574_-99+32577delinsGTAT
NM_007294.3:c.2834_2837delinsGTAT , LRG_292t1:c.2834_2837delinsGTAT	NP_009225.1:p.Ser945=
NM_007297.3:c.2693_2696delinsGTAT	NP_009228.2:p.Ser898=
NM_007298.3:c.788-1665_788-1662delinsGTAT	NP_009229.2:n.788-1665_788-1662delinsGTAT
NM_007299.3:c.788-1665_788-1662delinsGTAT	NP_009230.2:n.788-1665_788-1662delinsGTAT
NM_007300.3:c.2834_2837delinsGTAT	NP_009231.2:p.Ser945=
NR_027676.1:n.2970_2973delinsGTAT
NM_007294.4:c.2834_2837delinsGTAT MANE Select	NP_009225.1:p.Ser945=
NM_007297.4:c.2693_2696delinsGTAT	NP_009228.2:p.Ser898=
NM_007299.4:c.788-1665_788-1662delinsGTAT	NP_009230.2:n.788-1665_788-1662delinsGTAT
NM_007300.4:c.2834_2837delinsGTAT	NP_009231.2:p.Ser945=
NR_027676.2:n.3011_3014delinsGTAT