Canonical Allele Identifier: CA10592816

Gene: BRCA1

Linked Data

• dbSNP Id: rs587782606
• MyVariant Identifiers: chr17:g.41228628A>T (hg19) ; chr17:g.43076611A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43076611A>T , CM000679.2:g.43076611A>T	GRCh38
NC_000017.10:g.41228628A>T , CM000679.1:g.41228628A>T	GRCh37
NC_000017.9:g.38482154A>T	NCBI36
NG_005905.2:g.141373T>A , LRG_292:g.141373T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461574.2:c.4358T>A	ENSP00000417241.2:p.Val1453Glu
ENST00000470026.6:c.4361T>A	ENSP00000419274.2:p.Val1454Glu
ENST00000473961.6:c.4235T>A	ENSP00000420201.2:p.Val1412Glu
ENST00000476777.6:c.4355T>A	ENSP00000417554.2:p.Val1452Glu
ENST00000477152.6:c.4283T>A	ENSP00000419988.2:p.Val1428Glu
ENST00000478531.6:c.1049T>A	ENSP00000420412.2:p.Val350Glu
ENST00000489037.2:c.4283T>A	ENSP00000420781.2:p.Val1428Glu
ENST00000493919.6:c.911T>A	ENSP00000418819.2:p.Val304Glu
ENST00000494123.6:c.4361T>A	ENSP00000419103.2:p.Val1454Glu
ENST00000497488.2:c.3473T>A	ENSP00000418986.2:p.Val1158Glu
ENST00000618469.2:c.4361T>A	ENSP00000478114.2:p.Val1454Glu
ENST00000634433.2:c.4238T>A	ENSP00000489431.2:p.Val1413Glu
ENST00000644379.2:c.4427T>A	ENSP00000496570.2:p.Val1476Glu
ENST00000644555.2:c.911T>A	ENSP00000494614.2:p.Val304Glu
ENST00000652672.2:c.4220T>A	ENSP00000498906.2:p.Val1407Glu
ENST00000484087.6:c.923T>A	ENSP00000419481.2:p.Val308Glu
ENST00000700182.1:c.968T>A	ENSP00000514849.1:p.Val323Glu
ENST00000357654.9:c.4361T>A MANE Select	ENSP00000350283.3:p.Val1454Glu
ENST00000471181.7:c.4424T>A	ENSP00000418960.2:p.Val1475Glu
ENST00000644379.1:c.748T>A
ENST00000352993.7:c.935T>A	ENSP00000312236.5:p.Val312Glu
ENST00000357654.7:c.4361T>A	ENSP00000350283.3:p.Val1454Glu
ENST00000461221.5:c.*4144T>A	ENSP00000418548.1:n.*4144T>A
ENST00000461574.1:c.652T>A
ENST00000468300.5:c.1049T>A	ENSP00000417148.1:p.Val350Glu
ENST00000471181.6:c.4424T>A	ENSP00000418960.2:p.Val1475Glu
ENST00000478531.5:c.1049T>A	ENSP00000420412.1:p.Val350Glu
ENST00000484087.5:c.674T>A	ENSP00000419481.1:p.Val225Glu
ENST00000487825.5:c.677T>A	ENSP00000418212.1:p.Val226Glu
ENST00000491747.6:c.1049T>A	ENSP00000420705.2:p.Val350Glu
ENST00000493795.5:c.4220T>A	ENSP00000418775.1:p.Val1407Glu
ENST00000493919.5:c.911T>A	ENSP00000418819.1:p.Val304Glu
ENST00000586385.5:c.5-12660T>A	ENSP00000465818.1:n.5-12660T>A
ENST00000591534.5:c.-43-2090T>A	ENSP00000467329.1:n.-43-2090T>A
ENST00000591849.5:c.-98-26421T>A	ENSP00000465347.1:n.-98-26421T>A
ENST00000621897.1:n.252T>A
NM_007294.3:c.4361T>A , LRG_292t1:c.4361T>A	NP_009225.1:p.Val1454Glu
NM_007297.3:c.4220T>A	NP_009228.2:p.Val1407Glu
NM_007298.3:c.1049T>A	NP_009229.2:p.Val350Glu
NM_007299.3:c.1049T>A	NP_009230.2:p.Val350Glu
NM_007300.3:c.4424T>A	NP_009231.2:p.Val1475Glu
NR_027676.1:n.4497T>A
NM_007294.4:c.4361T>A MANE Select	NP_009225.1:p.Val1454Glu
NM_007297.4:c.4220T>A	NP_009228.2:p.Val1407Glu
NM_007299.4:c.1049T>A	NP_009230.2:p.Val350Glu
NM_007300.4:c.4424T>A	NP_009231.2:p.Val1475Glu
NR_027676.2:n.4538T>A