Canonical Allele Identifier: CA10593175

Gene: BRCA1

Linked Data

• dbSNP Id: rs2154153420
• MyVariant Identifiers: chr17:g.41234504G>C (hg19) ; chr17:g.43082487G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43082487G>C , CM000679.2:g.43082487G>C	GRCh38
NC_000017.10:g.41234504G>C , CM000679.1:g.41234504G>C	GRCh37
NC_000017.9:g.38488030G>C	NCBI36
NG_005905.2:g.135497C>G , LRG_292:g.135497C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000461574.2:c.4274C>G	ENSP00000417241.2:p.Pro1425Arg
ENST00000470026.6:c.4274C>G	ENSP00000419274.2:p.Pro1425Arg
ENST00000473961.6:c.4148C>G	ENSP00000420201.2:p.Pro1383Arg
ENST00000476777.6:c.4268C>G	ENSP00000417554.2:p.Pro1423Arg
ENST00000477152.6:c.4196C>G	ENSP00000419988.2:p.Pro1399Arg
ENST00000478531.6:c.962C>G	ENSP00000420412.2:p.Pro321Arg
ENST00000489037.2:c.4196C>G	ENSP00000420781.2:p.Pro1399Arg
ENST00000493919.6:c.824C>G	ENSP00000418819.2:p.Pro275Arg
ENST00000494123.6:c.4274C>G	ENSP00000419103.2:p.Pro1425Arg
ENST00000497488.2:c.3386C>G	ENSP00000418986.2:p.Pro1129Arg
ENST00000618469.2:c.4274C>G	ENSP00000478114.2:p.Pro1425Arg
ENST00000634433.2:c.4151C>G	ENSP00000489431.2:p.Pro1384Arg
ENST00000644379.2:c.4274C>G	ENSP00000496570.2:p.Pro1425Arg
ENST00000644555.2:c.824C>G	ENSP00000494614.2:p.Pro275Arg
ENST00000652672.2:c.4133C>G	ENSP00000498906.2:p.Pro1378Arg
ENST00000484087.6:c.839C>G	ENSP00000419481.2:p.Pro280Arg
ENST00000700182.1:c.884C>G	ENSP00000514849.1:p.Pro295Arg
ENST00000357654.9:c.4274C>G MANE Select	ENSP00000350283.3:p.Pro1425Arg
ENST00000471181.7:c.4274C>G	ENSP00000418960.2:p.Pro1425Arg
ENST00000644379.1:c.595C>G
ENST00000352993.7:c.848C>G	ENSP00000312236.5:p.Pro283Arg
ENST00000357654.7:c.4274C>G	ENSP00000350283.3:p.Pro1425Arg
ENST00000461221.5:c.*4057C>G	ENSP00000418548.1:n.*4057C>G
ENST00000461574.1:c.568C>G
ENST00000468300.5:c.965C>G	ENSP00000417148.1:p.Pro322Arg
ENST00000471181.6:c.4274C>G	ENSP00000418960.2:p.Pro1425Arg
ENST00000478531.5:c.962C>G	ENSP00000420412.1:p.Pro321Arg
ENST00000484087.5:c.587C>G	ENSP00000419481.1:p.Pro196Arg
ENST00000487825.5:c.590C>G	ENSP00000418212.1:p.Pro197Arg
ENST00000491747.6:c.965C>G	ENSP00000420705.2:p.Pro322Arg
ENST00000493795.5:c.4133C>G	ENSP00000418775.1:p.Pro1378Arg
ENST00000493919.5:c.824C>G	ENSP00000418819.1:p.Pro275Arg
ENST00000586385.5:c.5-18536C>G	ENSP00000465818.1:n.5-18536C>G
ENST00000591534.5:c.-43-7966C>G	ENSP00000467329.1:n.-43-7966C>G
ENST00000591849.5:c.-98-32297C>G	ENSP00000465347.1:n.-98-32297C>G
ENST00000621897.1:n.168C>G
NM_007294.3:c.4274C>G , LRG_292t1:c.4274C>G	NP_009225.1:p.Pro1425Arg
NM_007297.3:c.4133C>G	NP_009228.2:p.Pro1378Arg
NM_007298.3:c.965C>G	NP_009229.2:p.Pro322Arg
NM_007299.3:c.965C>G	NP_009230.2:p.Pro322Arg
NM_007300.3:c.4274C>G	NP_009231.2:p.Pro1425Arg
NR_027676.1:n.4410C>G
NM_007294.4:c.4274C>G MANE Select	NP_009225.1:p.Pro1425Arg
NM_007297.4:c.4133C>G	NP_009228.2:p.Pro1378Arg
NM_007299.4:c.965C>G	NP_009230.2:p.Pro322Arg
NM_007300.4:c.4274C>G	NP_009231.2:p.Pro1425Arg
NR_027676.2:n.4451C>G