Canonical Allele Identifier: CA052697

Gene: BRCA1

Linked Data

• dbSNP Id: rs762883588
• ExAC: 17:41226316 T / C
• gnomAD v2: 17-41226316-T-C
• gnomAD v3: 17-43074299-T-C
• gnomAD v4: 17-43074299-T-C
• MyVariant Identifiers: chr17:g.41226316T>C (hg19) ; chr17:g.43074299T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43074299T>C , CM000679.2:g.43074299T>C	GRCh38
NC_000017.10:g.41226316T>C , CM000679.1:g.41226316T>C	GRCh37
NC_000017.9:g.38479842T>C	NCBI36
NG_005905.2:g.143685A>G , LRG_292:g.143685A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461574.2:c.4672+32A>G	ENSP00000417241.2:n.4672+32A>G
ENST00000470026.6:c.4675+32A>G	ENSP00000419274.2:n.4675+32A>G
ENST00000473961.6:c.4549+32A>G	ENSP00000420201.2:n.4549+32A>G
ENST00000476777.6:c.4669+32A>G	ENSP00000417554.2:n.4669+32A>G
ENST00000477152.6:c.4597+32A>G	ENSP00000419988.2:n.4597+32A>G
ENST00000478531.6:c.1363+32A>G	ENSP00000420412.2:n.1363+32A>G
ENST00000489037.2:c.4597+32A>G	ENSP00000420781.2:n.4597+32A>G
ENST00000493919.6:c.1225+32A>G	ENSP00000418819.2:n.1225+32A>G
ENST00000494123.6:c.4675+32A>G	ENSP00000419103.2:n.4675+32A>G
ENST00000497488.2:c.3787+32A>G	ENSP00000418986.2:n.3787+32A>G
ENST00000618469.2:c.4675+32A>G	ENSP00000478114.2:n.4675+32A>G
ENST00000634433.2:c.4552+32A>G	ENSP00000489431.2:n.4552+32A>G
ENST00000644379.2:c.4741+32A>G	ENSP00000496570.2:n.4741+32A>G
ENST00000644555.2:c.1225+32A>G	ENSP00000494614.2:n.1225+32A>G
ENST00000652672.2:c.4534+32A>G	ENSP00000498906.2:n.4534+32A>G
ENST00000484087.6:c.1237+32A>G	ENSP00000419481.2:n.1237+32A>G
ENST00000700182.1:c.1282+32A>G	ENSP00000514849.1:n.1282+32A>G
ENST00000357654.9:c.4675+32A>G MANE Select	ENSP00000350283.3:n.4675+32A>G
ENST00000471181.7:c.4738+32A>G	ENSP00000418960.2:n.4738+32A>G
ENST00000644379.1:c.1062+32A>G
ENST00000352993.7:c.1249+32A>G	ENSP00000312236.5:n.1249+32A>G
ENST00000357654.7:c.4675+32A>G	ENSP00000350283.3:n.4675+32A>G
ENST00000461221.5:c.*4458+32A>G	ENSP00000418548.1:n.*4458+32A>G
ENST00000468300.5:c.1363+32A>G	ENSP00000417148.1:n.1363+32A>G
ENST00000471181.6:c.4738+32A>G	ENSP00000418960.2:n.4738+32A>G
ENST00000478531.5:c.1363+32A>G	ENSP00000420412.1:n.1363+32A>G
ENST00000484087.5:c.988+32A>G	ENSP00000419481.1:n.988+32A>G
ENST00000491747.6:c.1363+32A>G	ENSP00000420705.2:n.1363+32A>G
ENST00000493795.5:c.4534+32A>G	ENSP00000418775.1:n.4534+32A>G
ENST00000493919.5:c.1225+32A>G	ENSP00000418819.1:n.1225+32A>G
ENST00000586385.5:c.5-10348A>G	ENSP00000465818.1:n.5-10348A>G
ENST00000591534.5:c.148+32A>G	ENSP00000467329.1:n.148+32A>G
ENST00000591849.5:c.-98-24109A>G	ENSP00000465347.1:n.-98-24109A>G
NM_007294.3:c.4675+32A>G , LRG_292t1:c.4675+32A>G	NP_009225.1:n.4675+32A>G
NM_007297.3:c.4534+32A>G	NP_009228.2:n.4534+32A>G
NM_007298.3:c.1363+32A>G	NP_009229.2:n.1363+32A>G
NM_007299.3:c.1363+32A>G	NP_009230.2:n.1363+32A>G
NM_007300.3:c.4738+32A>G	NP_009231.2:n.4738+32A>G
NR_027676.1:n.4811+32A>G
NM_007294.4:c.4675+32A>G MANE Select	NP_009225.1:n.4675+32A>G
NM_007297.4:c.4534+32A>G	NP_009228.2:n.4534+32A>G
NM_007299.4:c.1363+32A>G	NP_009230.2:n.1363+32A>G
NM_007300.4:c.4738+32A>G	NP_009231.2:n.4738+32A>G
NR_027676.2:n.4852+32A>G