Canonical Allele Identifier: CA10600070

Gene: BRCA1

Linked Data

• dbSNP Id: rs80357140
• gnomAD v3: 17-43094538-C-A
• gnomAD v4: 17-43094538-C-A
• MyVariant Identifiers: chr17:g.41246555C>A (hg19) ; chr17:g.43094538C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43094538C>A , CM000679.2:g.43094538C>A	GRCh38
NC_000017.10:g.41246555C>A , CM000679.1:g.41246555C>A	GRCh37
NC_000017.9:g.38500081C>A	NCBI36
NG_005905.2:g.123446G>T , LRG_292:g.123446G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354071.8:n.1057G>T
ENST00000461574.2:c.993G>T	ENSP00000417241.2:p.Arg331Ser
ENST00000470026.6:c.993G>T	ENSP00000419274.2:p.Arg331Ser
ENST00000473961.6:c.867G>T	ENSP00000420201.2:p.Arg289Ser
ENST00000476777.6:c.990G>T	ENSP00000417554.2:p.Arg330Ser
ENST00000477152.6:c.915G>T	ENSP00000419988.2:p.Arg305Ser
ENST00000478531.6:c.784+206G>T	ENSP00000420412.2:n.784+206G>T
ENST00000489037.2:c.915G>T	ENSP00000420781.2:p.Arg305Ser
ENST00000493919.6:c.646+206G>T	ENSP00000418819.2:n.646+206G>T
ENST00000494123.6:c.993G>T	ENSP00000419103.2:p.Arg331Ser
ENST00000497488.2:c.105G>T	ENSP00000418986.2:p.Arg35Ser
ENST00000618469.2:c.993G>T	ENSP00000478114.2:p.Arg331Ser
ENST00000634433.2:c.870G>T	ENSP00000489431.2:p.Arg290Ser
ENST00000644379.2:c.993G>T	ENSP00000496570.2:p.Arg331Ser
ENST00000644555.2:c.646+206G>T	ENSP00000494614.2:n.646+206G>T
ENST00000652672.2:c.852G>T	ENSP00000498906.2:p.Arg284Ser
ENST00000484087.6:c.664+206G>T	ENSP00000419481.2:n.664+206G>T
ENST00000700182.1:c.706+206G>T	ENSP00000514849.1:n.706+206G>T
ENST00000700183.1:c.*1001G>T	ENSP00000514850.1:n.*1001G>T
ENST00000357654.9:c.993G>T MANE Select	ENSP00000350283.3:p.Arg331Ser
ENST00000471181.7:c.993G>T	ENSP00000418960.2:p.Arg331Ser
ENST00000642945.1:c.*867G>T	ENSP00000495897.1:n.*867G>T
ENST00000652672.1:c.852G>T	ENSP00000498906.1:p.Arg284Ser
ENST00000352993.7:c.670+1308G>T	ENSP00000312236.5:n.670+1308G>T
ENST00000354071.7:c.993G>T	ENSP00000326002.7:p.Arg331Ser
ENST00000357654.7:c.993G>T	ENSP00000350283.3:p.Arg331Ser
ENST00000412061.3:c.344G>T
ENST00000461221.5:c.*776G>T	ENSP00000418548.1:n.*776G>T
ENST00000468300.5:c.787+206G>T	ENSP00000417148.1:n.787+206G>T
ENST00000470026.5:c.993G>T	ENSP00000419274.1:p.Arg331Ser
ENST00000471181.6:c.993G>T	ENSP00000418960.2:p.Arg331Ser
ENST00000473961.5:c.590G>T
ENST00000477152.5:c.915G>T	ENSP00000419988.1:p.Arg305Ser
ENST00000478531.5:c.784+206G>T	ENSP00000420412.1:n.784+206G>T
ENST00000484087.5:c.409+206G>T	ENSP00000419481.1:n.409+206G>T
ENST00000487825.5:c.412+206G>T	ENSP00000418212.1:n.412+206G>T
ENST00000491747.6:c.787+206G>T	ENSP00000420705.2:n.787+206G>T
ENST00000492859.5:c.*929G>T	ENSP00000420253.1:n.*929G>T
ENST00000493795.5:c.852G>T	ENSP00000418775.1:p.Arg284Ser
ENST00000493919.5:c.646+206G>T	ENSP00000418819.1:n.646+206G>T
ENST00000494123.5:c.993G>T	ENSP00000419103.1:p.Arg331Ser
ENST00000497488.1:c.105G>T	ENSP00000418986.1:p.Arg35Ser
ENST00000586385.5:c.5-30587G>T	ENSP00000465818.1:n.5-30587G>T
ENST00000591534.5:c.-43-20017G>T	ENSP00000467329.1:n.-43-20017G>T
ENST00000591849.5:c.-99+30733G>T	ENSP00000465347.1:n.-99+30733G>T
ENST00000634433.1:c.870G>T	ENSP00000489431.1:p.Arg290Ser
NM_007294.3:c.993G>T , LRG_292t1:c.993G>T	NP_009225.1:p.Arg331Ser
NM_007297.3:c.852G>T	NP_009228.2:p.Arg284Ser
NM_007298.3:c.787+206G>T	NP_009229.2:n.787+206G>T
NM_007299.3:c.787+206G>T	NP_009230.2:n.787+206G>T
NM_007300.3:c.993G>T	NP_009231.2:p.Arg331Ser
NR_027676.1:n.1129G>T
NM_007294.4:c.993G>T MANE Select	NP_009225.1:p.Arg331Ser
NM_007297.4:c.852G>T	NP_009228.2:p.Arg284Ser
NM_007299.4:c.787+206G>T	NP_009230.2:n.787+206G>T
NM_007300.4:c.993G>T	NP_009231.2:p.Arg331Ser
NR_027676.2:n.1170G>T