Canonical Allele Identifier: CA10591903

Gene: BRCA1

Linked Data

• dbSNP Id: rs1064794054
• gnomAD v4: 17-43071106-G-C
• MyVariant Identifiers: chr17:g.41223123G>C (hg19) ; chr17:g.43071106G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43071106G>C , CM000679.2:g.43071106G>C	GRCh38
NC_000017.10:g.41223123G>C , CM000679.1:g.41223123G>C	GRCh37
NC_000017.9:g.38476649G>C	NCBI36
NG_005905.2:g.146878C>G , LRG_292:g.146878C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461574.2:c.4805C>G	ENSP00000417241.2:p.Pro1602Arg
ENST00000470026.6:c.4808C>G	ENSP00000419274.2:p.Pro1603Arg
ENST00000473961.6:c.4682C>G	ENSP00000420201.2:p.Pro1561Arg
ENST00000476777.6:c.4802C>G	ENSP00000417554.2:p.Pro1601Arg
ENST00000477152.6:c.4730C>G	ENSP00000419988.2:p.Pro1577Arg
ENST00000478531.6:c.1496C>G	ENSP00000420412.2:p.Pro499Arg
ENST00000489037.2:c.4730C>G	ENSP00000420781.2:p.Pro1577Arg
ENST00000493919.6:c.1358C>G	ENSP00000418819.2:p.Pro453Arg
ENST00000494123.6:c.4808C>G	ENSP00000419103.2:p.Pro1603Arg
ENST00000497488.2:c.3920C>G	ENSP00000418986.2:p.Pro1307Arg
ENST00000618469.2:c.4808C>G	ENSP00000478114.2:p.Pro1603Arg
ENST00000634433.2:c.4685C>G	ENSP00000489431.2:p.Pro1562Arg
ENST00000644379.2:c.4874C>G	ENSP00000496570.2:p.Pro1625Arg
ENST00000644555.2:c.1358C>G	ENSP00000494614.2:p.Pro453Arg
ENST00000652672.2:c.4667C>G	ENSP00000498906.2:p.Pro1556Arg
ENST00000484087.6:c.1370C>G	ENSP00000419481.2:p.Pro457Arg
ENST00000700182.1:c.1415C>G	ENSP00000514849.1:p.Pro472Arg
ENST00000357654.9:c.4808C>G MANE Select	ENSP00000350283.3:p.Pro1603Arg
ENST00000471181.7:c.4871C>G	ENSP00000418960.2:p.Pro1624Arg
ENST00000644379.1:c.1195C>G
ENST00000352993.7:c.1382C>G	ENSP00000312236.5:p.Pro461Arg
ENST00000357654.7:c.4808C>G	ENSP00000350283.3:p.Pro1603Arg
ENST00000461221.5:c.*4591C>G	ENSP00000418548.1:n.*4591C>G
ENST00000468300.5:c.1496C>G	ENSP00000417148.1:p.Pro499Arg
ENST00000471181.6:c.4871C>G	ENSP00000418960.2:p.Pro1624Arg
ENST00000478531.5:c.1496C>G	ENSP00000420412.1:p.Pro499Arg
ENST00000484087.5:c.1121C>G	ENSP00000419481.1:p.Pro374Arg
ENST00000491747.6:c.1496C>G	ENSP00000420705.2:p.Pro499Arg
ENST00000493795.5:c.4667C>G	ENSP00000418775.1:p.Pro1556Arg
ENST00000493919.5:c.1358C>G	ENSP00000418819.1:p.Pro453Arg
ENST00000586385.5:c.5-7155C>G	ENSP00000465818.1:n.5-7155C>G
ENST00000591534.5:c.281C>G	ENSP00000467329.1:p.Pro94Arg
ENST00000591849.5:c.-98-20916C>G	ENSP00000465347.1:n.-98-20916C>G
NM_007294.3:c.4808C>G , LRG_292t1:c.4808C>G	NP_009225.1:p.Pro1603Arg
NM_007297.3:c.4667C>G	NP_009228.2:p.Pro1556Arg
NM_007298.3:c.1496C>G	NP_009229.2:p.Pro499Arg
NM_007299.3:c.1496C>G	NP_009230.2:p.Pro499Arg
NM_007300.3:c.4871C>G	NP_009231.2:p.Pro1624Arg
NR_027676.1:n.4944C>G
NM_007294.4:c.4808C>G MANE Select	NP_009225.1:p.Pro1603Arg
NM_007297.4:c.4667C>G	NP_009228.2:p.Pro1556Arg
NM_007299.4:c.1496C>G	NP_009230.2:p.Pro499Arg
NM_007300.4:c.4871C>G	NP_009231.2:p.Pro1624Arg
NR_027676.2:n.4985C>G