Canonical Allele Identifier: CA10593173

Gene: BRCA1

Linked Data

• dbSNP Id: rs2154153319
• MyVariant Identifiers: chr17:g.41234502A>T (hg19) ; chr17:g.43082485A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43082485A>T , CM000679.2:g.43082485A>T	GRCh38
NC_000017.10:g.41234502A>T , CM000679.1:g.41234502A>T	GRCh37
NC_000017.9:g.38488028A>T	NCBI36
NG_005905.2:g.135499T>A , LRG_292:g.135499T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000461574.2:c.4276T>A	ENSP00000417241.2:p.Ser1426Thr
ENST00000470026.6:c.4276T>A	ENSP00000419274.2:p.Ser1426Thr
ENST00000473961.6:c.4150T>A	ENSP00000420201.2:p.Ser1384Thr
ENST00000476777.6:c.4270T>A	ENSP00000417554.2:p.Ser1424Thr
ENST00000477152.6:c.4198T>A	ENSP00000419988.2:p.Ser1400Thr
ENST00000478531.6:c.964T>A	ENSP00000420412.2:p.Ser322Thr
ENST00000489037.2:c.4198T>A	ENSP00000420781.2:p.Ser1400Thr
ENST00000493919.6:c.826T>A	ENSP00000418819.2:p.Ser276Thr
ENST00000494123.6:c.4276T>A	ENSP00000419103.2:p.Ser1426Thr
ENST00000497488.2:c.3388T>A	ENSP00000418986.2:p.Ser1130Thr
ENST00000618469.2:c.4276T>A	ENSP00000478114.2:p.Ser1426Thr
ENST00000634433.2:c.4153T>A	ENSP00000489431.2:p.Ser1385Thr
ENST00000644379.2:c.4276T>A	ENSP00000496570.2:p.Ser1426Thr
ENST00000644555.2:c.826T>A	ENSP00000494614.2:p.Ser276Thr
ENST00000652672.2:c.4135T>A	ENSP00000498906.2:p.Ser1379Thr
ENST00000484087.6:c.841T>A	ENSP00000419481.2:p.Ser281Thr
ENST00000700182.1:c.886T>A	ENSP00000514849.1:p.Ser296Thr
ENST00000357654.9:c.4276T>A MANE Select	ENSP00000350283.3:p.Ser1426Thr
ENST00000471181.7:c.4276T>A	ENSP00000418960.2:p.Ser1426Thr
ENST00000644379.1:c.597T>A
ENST00000352993.7:c.850T>A	ENSP00000312236.5:p.Ser284Thr
ENST00000357654.7:c.4276T>A	ENSP00000350283.3:p.Ser1426Thr
ENST00000461221.5:c.*4059T>A	ENSP00000418548.1:n.*4059T>A
ENST00000461574.1:c.570T>A
ENST00000468300.5:c.967T>A	ENSP00000417148.1:p.Ser323Thr
ENST00000471181.6:c.4276T>A	ENSP00000418960.2:p.Ser1426Thr
ENST00000478531.5:c.964T>A	ENSP00000420412.1:p.Ser322Thr
ENST00000484087.5:c.589T>A	ENSP00000419481.1:p.Ser197Thr
ENST00000487825.5:c.592T>A	ENSP00000418212.1:p.Ser198Thr
ENST00000491747.6:c.967T>A	ENSP00000420705.2:p.Ser323Thr
ENST00000493795.5:c.4135T>A	ENSP00000418775.1:p.Ser1379Thr
ENST00000493919.5:c.826T>A	ENSP00000418819.1:p.Ser276Thr
ENST00000586385.5:c.5-18534T>A	ENSP00000465818.1:n.5-18534T>A
ENST00000591534.5:c.-43-7964T>A	ENSP00000467329.1:n.-43-7964T>A
ENST00000591849.5:c.-98-32295T>A	ENSP00000465347.1:n.-98-32295T>A
ENST00000621897.1:n.170T>A
NM_007294.3:c.4276T>A , LRG_292t1:c.4276T>A	NP_009225.1:p.Ser1426Thr
NM_007297.3:c.4135T>A	NP_009228.2:p.Ser1379Thr
NM_007298.3:c.967T>A	NP_009229.2:p.Ser323Thr
NM_007299.3:c.967T>A	NP_009230.2:p.Ser323Thr
NM_007300.3:c.4276T>A	NP_009231.2:p.Ser1426Thr
NR_027676.1:n.4412T>A
NM_007294.4:c.4276T>A MANE Select	NP_009225.1:p.Ser1426Thr
NM_007297.4:c.4135T>A	NP_009228.2:p.Ser1379Thr
NM_007299.4:c.967T>A	NP_009230.2:p.Ser323Thr
NM_007300.4:c.4276T>A	NP_009231.2:p.Ser1426Thr
NR_027676.2:n.4453T>A