Canonical Allele Identifier: CA919844518

Gene: BRCA1

Linked Data

• dbSNP Id: rs1567792012

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43092178_43092184dup , CM000679.2:g.43092178_43092184dup	GRCh38
NC_000017.10:g.41244195_41244201dup , CM000679.1:g.41244195_41244201dup	GRCh37
NC_000017.9:g.38497721_38497727dup	NCBI36
NG_005905.2:g.125800_125806dup , LRG_292:g.125800_125806dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354071.8:n.3411_3417dup
ENST00000461574.2:c.3347_3353dup	ENSP00000417241.2:p.Gln1118HisfsTer6
ENST00000470026.6:c.3347_3353dup	ENSP00000419274.2:p.Gln1118HisfsTer6
ENST00000473961.6:c.3221_3227dup	ENSP00000420201.2:p.Gln1076HisfsTer6
ENST00000476777.6:c.3344_3350dup	ENSP00000417554.2:p.Gln1117HisfsTer6
ENST00000477152.6:c.3269_3275dup	ENSP00000419988.2:p.Gln1092HisfsTer6
ENST00000478531.6:c.785-1152_785-1146dup	ENSP00000420412.2:n.785-1152_785-1146dup
ENST00000489037.2:c.3269_3275dup	ENSP00000420781.2:p.Gln1092HisfsTer6
ENST00000493919.6:c.647-1152_647-1146dup	ENSP00000418819.2:n.647-1152_647-1146dup
ENST00000494123.6:c.3347_3353dup	ENSP00000419103.2:p.Gln1118HisfsTer6
ENST00000497488.2:c.2459_2465dup	ENSP00000418986.2:p.Gln822HisfsTer6
ENST00000618469.2:c.3347_3353dup	ENSP00000478114.2:p.Gln1118HisfsTer6
ENST00000634433.2:c.3224_3230dup	ENSP00000489431.2:p.Gln1077HisfsTer6
ENST00000644379.2:c.3347_3353dup	ENSP00000496570.2:p.Gln1118HisfsTer6
ENST00000644555.2:c.647-1152_647-1146dup	ENSP00000494614.2:n.647-1152_647-1146dup
ENST00000652672.2:c.3206_3212dup	ENSP00000498906.2:p.Gln1071HisfsTer6
ENST00000484087.6:c.665-1152_665-1146dup	ENSP00000419481.2:n.665-1152_665-1146dup
ENST00000700182.1:c.707-1152_707-1146dup	ENSP00000514849.1:n.707-1152_707-1146dup
ENST00000357654.9:c.3347_3353dup MANE Select	ENSP00000350283.3:p.Gln1118HisfsTer6
ENST00000471181.7:c.3347_3353dup	ENSP00000418960.2:p.Gln1118HisfsTer6
ENST00000352993.7:c.671-1152_671-1146dup	ENSP00000312236.5:n.671-1152_671-1146dup
ENST00000354071.7:c.3347_3353dup	ENSP00000326002.7:p.Gln1118HisfsTer6
ENST00000357654.7:c.3347_3353dup	ENSP00000350283.3:p.Gln1118HisfsTer6
ENST00000461221.5:c.*3130_*3136dup	ENSP00000418548.1:n.*3130_*3136dup
ENST00000468300.5:c.788-1152_788-1146dup	ENSP00000417148.1:n.788-1152_788-1146dup
ENST00000471181.6:c.3347_3353dup	ENSP00000418960.2:p.Gln1118HisfsTer6
ENST00000478531.5:c.785-1152_785-1146dup	ENSP00000420412.1:n.785-1152_785-1146dup
ENST00000484087.5:c.410-1152_410-1146dup	ENSP00000419481.1:n.410-1152_410-1146dup
ENST00000487825.5:c.413-1152_413-1146dup	ENSP00000418212.1:n.413-1152_413-1146dup
ENST00000491747.6:c.788-1152_788-1146dup	ENSP00000420705.2:n.788-1152_788-1146dup
ENST00000493795.5:c.3206_3212dup	ENSP00000418775.1:p.Gln1071HisfsTer6
ENST00000493919.5:c.647-1152_647-1146dup	ENSP00000418819.1:n.647-1152_647-1146dup
ENST00000586385.5:c.5-28233_5-28227dup	ENSP00000465818.1:n.5-28233_5-28227dup
ENST00000591534.5:c.-43-17663_-43-17657dup	ENSP00000467329.1:n.-43-17663_-43-17657dup
ENST00000591849.5:c.-99+33087_-99+33093dup	ENSP00000465347.1:n.-99+33087_-99+33093dup
NM_007294.3:c.3347_3353dup , LRG_292t1:c.3347_3353dup	NP_009225.1:p.Gln1118HisfsTer6
NM_007297.3:c.3206_3212dup	NP_009228.2:p.Gln1071HisfsTer6
NM_007298.3:c.788-1152_788-1146dup	NP_009229.2:n.788-1152_788-1146dup
NM_007299.3:c.788-1152_788-1146dup	NP_009230.2:n.788-1152_788-1146dup
NM_007300.3:c.3347_3353dup	NP_009231.2:p.Gln1118HisfsTer6
NR_027676.1:n.3483_3489dup
NM_007294.4:c.3347_3353dup MANE Select	NP_009225.1:p.Gln1118HisfsTer6
NM_007297.4:c.3206_3212dup	NP_009228.2:p.Gln1071HisfsTer6
NM_007299.4:c.788-1152_788-1146dup	NP_009230.2:n.788-1152_788-1146dup
NM_007300.4:c.3347_3353dup	NP_009231.2:p.Gln1118HisfsTer6
NR_027676.2:n.3524_3530dup