Canonical Allele Identifier: CA2260784877

Gene: BRCA1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43094390_43094391delinsTC , CM000679.2:g.43094390_43094391delinsTC	GRCh38
NC_000017.10:g.41246407_41246408delinsTC , CM000679.1:g.41246407_41246408delinsTC	GRCh37
NC_000017.9:g.38499933_38499934delinsTC	NCBI36
NG_005905.2:g.123593_123594delinsGA , LRG_292:g.123593_123594delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354071.8:n.1204_1205delinsGA
ENST00000461574.2:c.1140_1141delinsGA	ENSP00000417241.2:p.Gln380=
ENST00000470026.6:c.1140_1141delinsGA	ENSP00000419274.2:p.Gln380=
ENST00000473961.6:c.1014_1015delinsGA	ENSP00000420201.2:p.Gln338=
ENST00000476777.6:c.1137_1138delinsGA	ENSP00000417554.2:p.Gln379=
ENST00000477152.6:c.1062_1063delinsGA	ENSP00000419988.2:p.Gln354=
ENST00000478531.6:c.784+353_784+354delinsGA	ENSP00000420412.2:n.784+353_784+354delinsGA
ENST00000489037.2:c.1062_1063delinsGA	ENSP00000420781.2:p.Gln354=
ENST00000493919.6:c.646+353_646+354delinsGA	ENSP00000418819.2:n.646+353_646+354delinsGA
ENST00000494123.6:c.1140_1141delinsGA	ENSP00000419103.2:p.Gln380=
ENST00000497488.2:c.252_253delinsGA	ENSP00000418986.2:p.Gln84=
ENST00000618469.2:c.1140_1141delinsGA	ENSP00000478114.2:p.Gln380=
ENST00000634433.2:c.1017_1018delinsGA	ENSP00000489431.2:p.Gln339=
ENST00000644379.2:c.1140_1141delinsGA	ENSP00000496570.2:p.Gln380=
ENST00000644555.2:c.646+353_646+354delinsGA	ENSP00000494614.2:n.646+353_646+354delinsGA
ENST00000652672.2:c.999_1000delinsGA	ENSP00000498906.2:p.Gln333=
ENST00000484087.6:c.664+353_664+354delinsGA	ENSP00000419481.2:n.664+353_664+354delinsGA
ENST00000700182.1:c.706+353_706+354delinsGA	ENSP00000514849.1:n.706+353_706+354delinsGA
ENST00000700183.1:c.*1148_*1149delinsGA	ENSP00000514850.1:n.*1148_*1149delinsGA
ENST00000357654.9:c.1140_1141delinsGA MANE Select	ENSP00000350283.3:p.Gln380=
ENST00000471181.7:c.1140_1141delinsGA	ENSP00000418960.2:p.Gln380=
ENST00000652672.1:c.999_1000delinsGA	ENSP00000498906.1:p.Gln333=
ENST00000352993.7:c.670+1455_670+1456delinsGA	ENSP00000312236.5:n.670+1455_670+1456delinsGA
ENST00000354071.7:c.1140_1141delinsGA	ENSP00000326002.7:p.Gln380=
ENST00000357654.7:c.1140_1141delinsGA	ENSP00000350283.3:p.Gln380=
ENST00000412061.3:c.491_492delinsGA
ENST00000461221.5:c.*923_*924delinsGA	ENSP00000418548.1:n.*923_*924delinsGA
ENST00000468300.5:c.787+353_787+354delinsGA	ENSP00000417148.1:n.787+353_787+354delinsGA
ENST00000470026.5:c.1140_1141delinsGA	ENSP00000419274.1:p.Gln380=
ENST00000471181.6:c.1140_1141delinsGA	ENSP00000418960.2:p.Gln380=
ENST00000473961.5:c.737_738delinsGA
ENST00000477152.5:c.1062_1063delinsGA	ENSP00000419988.1:p.Gln354=
ENST00000478531.5:c.784+353_784+354delinsGA	ENSP00000420412.1:n.784+353_784+354delinsGA
ENST00000484087.5:c.409+353_409+354delinsGA	ENSP00000419481.1:n.409+353_409+354delinsGA
ENST00000487825.5:c.412+353_412+354delinsGA	ENSP00000418212.1:n.412+353_412+354delinsGA
ENST00000491747.6:c.787+353_787+354delinsGA	ENSP00000420705.2:n.787+353_787+354delinsGA
ENST00000492859.5:c.*1076_*1077delinsGA	ENSP00000420253.1:n.*1076_*1077delinsGA
ENST00000493795.5:c.999_1000delinsGA	ENSP00000418775.1:p.Gln333=
ENST00000493919.5:c.646+353_646+354delinsGA	ENSP00000418819.1:n.646+353_646+354delinsGA
ENST00000494123.5:c.1140_1141delinsGA	ENSP00000419103.1:p.Gln380=
ENST00000497488.1:c.252_253delinsGA	ENSP00000418986.1:p.Gln84=
ENST00000586385.5:c.5-30440_5-30439delinsGA	ENSP00000465818.1:n.5-30440_5-30439delinsGA
ENST00000591534.5:c.-43-19870_-43-19869delinsGA	ENSP00000467329.1:n.-43-19870_-43-19869delinsGA
ENST00000591849.5:c.-99+30880_-99+30881delinsGA	ENSP00000465347.1:n.-99+30880_-99+30881delinsGA
ENST00000634433.1:c.1017_1018delinsGA	ENSP00000489431.1:p.Gln339=
NM_007294.3:c.1140_1141delinsGA , LRG_292t1:c.1140_1141delinsGA	NP_009225.1:p.Gln380=
NM_007297.3:c.999_1000delinsGA	NP_009228.2:p.Gln333=
NM_007298.3:c.787+353_787+354delinsGA	NP_009229.2:n.787+353_787+354delinsGA
NM_007299.3:c.787+353_787+354delinsGA	NP_009230.2:n.787+353_787+354delinsGA
NM_007300.3:c.1140_1141delinsGA	NP_009231.2:p.Gln380=
NR_027676.1:n.1276_1277delinsGA
NM_007294.4:c.1140_1141delinsGA MANE Select	NP_009225.1:p.Gln380=
NM_007297.4:c.999_1000delinsGA	NP_009228.2:p.Gln333=
NM_007299.4:c.787+353_787+354delinsGA	NP_009230.2:n.787+353_787+354delinsGA
NM_007300.4:c.1140_1141delinsGA	NP_009231.2:p.Gln380=
NR_027676.2:n.1317_1318delinsGA