Canonical Allele Identifier: CA2260784886

Gene: BRCA1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43094397_43094398delinsGC , CM000679.2:g.43094397_43094398delinsGC	GRCh38
NC_000017.10:g.41246414_41246415delinsGC , CM000679.1:g.41246414_41246415delinsGC	GRCh37
NC_000017.9:g.38499940_38499941delinsGC	NCBI36
NG_005905.2:g.123586_123587delinsGC , LRG_292:g.123586_123587delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354071.8:n.1197_1198delinsGC
ENST00000461574.2:c.1133_1134delinsGC	ENSP00000417241.2:p.Ser378=
ENST00000470026.6:c.1133_1134delinsGC	ENSP00000419274.2:p.Ser378=
ENST00000473961.6:c.1007_1008delinsGC	ENSP00000420201.2:p.Ser336=
ENST00000476777.6:c.1130_1131delinsGC	ENSP00000417554.2:p.Ser377=
ENST00000477152.6:c.1055_1056delinsGC	ENSP00000419988.2:p.Ser352=
ENST00000478531.6:c.784+346_784+347delinsGC	ENSP00000420412.2:n.784+346_784+347delinsGC
ENST00000489037.2:c.1055_1056delinsGC	ENSP00000420781.2:p.Ser352=
ENST00000493919.6:c.646+346_646+347delinsGC	ENSP00000418819.2:n.646+346_646+347delinsGC
ENST00000494123.6:c.1133_1134delinsGC	ENSP00000419103.2:p.Ser378=
ENST00000497488.2:c.245_246delinsGC	ENSP00000418986.2:p.Ser82=
ENST00000618469.2:c.1133_1134delinsGC	ENSP00000478114.2:p.Ser378=
ENST00000634433.2:c.1010_1011delinsGC	ENSP00000489431.2:p.Ser337=
ENST00000644379.2:c.1133_1134delinsGC	ENSP00000496570.2:p.Ser378=
ENST00000644555.2:c.646+346_646+347delinsGC	ENSP00000494614.2:n.646+346_646+347delinsGC
ENST00000652672.2:c.992_993delinsGC	ENSP00000498906.2:p.Ser331=
ENST00000484087.6:c.664+346_664+347delinsGC	ENSP00000419481.2:n.664+346_664+347delinsGC
ENST00000700182.1:c.706+346_706+347delinsGC	ENSP00000514849.1:n.706+346_706+347delinsGC
ENST00000700183.1:c.*1141_*1142delinsGC	ENSP00000514850.1:n.*1141_*1142delinsGC
ENST00000357654.9:c.1133_1134delinsGC MANE Select	ENSP00000350283.3:p.Ser378=
ENST00000471181.7:c.1133_1134delinsGC	ENSP00000418960.2:p.Ser378=
ENST00000652672.1:c.992_993delinsGC	ENSP00000498906.1:p.Ser331=
ENST00000352993.7:c.670+1448_670+1449delinsGC	ENSP00000312236.5:n.670+1448_670+1449delinsGC
ENST00000354071.7:c.1133_1134delinsGC	ENSP00000326002.7:p.Ser378=
ENST00000357654.7:c.1133_1134delinsGC	ENSP00000350283.3:p.Ser378=
ENST00000412061.3:c.484_485delinsGC
ENST00000461221.5:c.*916_*917delinsGC	ENSP00000418548.1:n.*916_*917delinsGC
ENST00000468300.5:c.787+346_787+347delinsGC	ENSP00000417148.1:n.787+346_787+347delinsGC
ENST00000470026.5:c.1133_1134delinsGC	ENSP00000419274.1:p.Ser378=
ENST00000471181.6:c.1133_1134delinsGC	ENSP00000418960.2:p.Ser378=
ENST00000473961.5:c.730_731delinsGC
ENST00000477152.5:c.1055_1056delinsGC	ENSP00000419988.1:p.Ser352=
ENST00000478531.5:c.784+346_784+347delinsGC	ENSP00000420412.1:n.784+346_784+347delinsGC
ENST00000484087.5:c.409+346_409+347delinsGC	ENSP00000419481.1:n.409+346_409+347delinsGC
ENST00000487825.5:c.412+346_412+347delinsGC	ENSP00000418212.1:n.412+346_412+347delinsGC
ENST00000491747.6:c.787+346_787+347delinsGC	ENSP00000420705.2:n.787+346_787+347delinsGC
ENST00000492859.5:c.*1069_*1070delinsGC	ENSP00000420253.1:n.*1069_*1070delinsGC
ENST00000493795.5:c.992_993delinsGC	ENSP00000418775.1:p.Ser331=
ENST00000493919.5:c.646+346_646+347delinsGC	ENSP00000418819.1:n.646+346_646+347delinsGC
ENST00000494123.5:c.1133_1134delinsGC	ENSP00000419103.1:p.Ser378=
ENST00000497488.1:c.245_246delinsGC	ENSP00000418986.1:p.Ser82=
ENST00000586385.5:c.5-30447_5-30446delinsGC	ENSP00000465818.1:n.5-30447_5-30446delinsGC
ENST00000591534.5:c.-43-19877_-43-19876delinsGC	ENSP00000467329.1:n.-43-19877_-43-19876delinsGC
ENST00000591849.5:c.-99+30873_-99+30874delinsGC	ENSP00000465347.1:n.-99+30873_-99+30874delinsGC
ENST00000634433.1:c.1010_1011delinsGC	ENSP00000489431.1:p.Ser337=
NM_007294.3:c.1133_1134delinsGC , LRG_292t1:c.1133_1134delinsGC	NP_009225.1:p.Ser378=
NM_007297.3:c.992_993delinsGC	NP_009228.2:p.Ser331=
NM_007298.3:c.787+346_787+347delinsGC	NP_009229.2:n.787+346_787+347delinsGC
NM_007299.3:c.787+346_787+347delinsGC	NP_009230.2:n.787+346_787+347delinsGC
NM_007300.3:c.1133_1134delinsGC	NP_009231.2:p.Ser378=
NR_027676.1:n.1269_1270delinsGC
NM_007294.4:c.1133_1134delinsGC MANE Select	NP_009225.1:p.Ser378=
NM_007297.4:c.992_993delinsGC	NP_009228.2:p.Ser331=
NM_007299.4:c.787+346_787+347delinsGC	NP_009230.2:n.787+346_787+347delinsGC
NM_007300.4:c.1133_1134delinsGC	NP_009231.2:p.Ser378=
NR_027676.2:n.1310_1311delinsGC