Canonical Allele Identifier: CA003698

Gene: BRCA1

Linked Data

• ClinVar Variation Id: 182082
• ClinVar RCV Id: RCV000159854 ; RCV000466347 ; RCV001076357 ; RCV002345550
• dbSNP Id: rs730881447
• MyVariant Identifiers: chr17:g.41197759G>T (hg19) ; chr17:g.43045742G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43045742G>T , CM000679.2:g.43045742G>T	GRCh38
NC_000017.10:g.41197759G>T , CM000679.1:g.41197759G>T	GRCh37
NC_000017.9:g.38451285G>T	NCBI36
NG_005905.2:g.172242C>A , LRG_292:g.172242C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461574.2:c.5525C>A	ENSP00000417241.2:p.Ala1842Glu
ENST00000470026.6:c.5528C>A	ENSP00000419274.2:p.Ala1843Glu
ENST00000473961.6:c.5402C>A	ENSP00000420201.2:p.Ala1801Glu
ENST00000476777.6:c.5522C>A	ENSP00000417554.2:p.Ala1841Glu
ENST00000477152.6:c.5450C>A	ENSP00000419988.2:p.Ala1817Glu
ENST00000478531.6:c.2216C>A	ENSP00000420412.2:p.Ala739Glu
ENST00000489037.2:c.5450C>A	ENSP00000420781.2:p.Ala1817Glu
ENST00000493919.6:c.2078C>A	ENSP00000418819.2:p.Ala693Glu
ENST00000494123.6:c.5528C>A	ENSP00000419103.2:p.Ala1843Glu
ENST00000497488.2:c.4640C>A	ENSP00000418986.2:p.Ala1547Glu
ENST00000618469.2:c.5528C>A	ENSP00000478114.2:p.Ala1843Glu
ENST00000634433.2:c.5405C>A	ENSP00000489431.2:p.Ala1802Glu
ENST00000644379.2:c.5594C>A	ENSP00000496570.2:p.Ala1865Glu
ENST00000644555.2:c.2078C>A	ENSP00000494614.2:p.Ala693Glu
ENST00000652672.2:c.5387C>A	ENSP00000498906.2:p.Ala1796Glu
ENST00000484087.6:c.2090C>A	ENSP00000419481.2:p.Ala697Glu
ENST00000700081.1:n.1411C>A
ENST00000700082.1:n.892C>A
ENST00000357654.9:c.5528C>A MANE Select	ENSP00000350283.3:p.Ala1843Glu
ENST00000471181.7:c.5591C>A	ENSP00000418960.2:p.Ala1864Glu
ENST00000644379.1:c.1915C>A
ENST00000352993.7:c.2102C>A	ENSP00000312236.5:p.Ala701Glu
ENST00000357654.7:c.5528C>A	ENSP00000350283.3:p.Ala1843Glu
ENST00000461221.5:c.*5311C>A	ENSP00000418548.1:n.*5311C>A
ENST00000468300.5:c.*42C>A	ENSP00000417148.1:n.*42C>A
ENST00000471181.6:c.5591C>A	ENSP00000418960.2:p.Ala1864Glu
ENST00000491747.6:c.2216C>A	ENSP00000420705.2:p.Ala739Glu
ENST00000493795.5:c.5387C>A	ENSP00000418775.1:p.Ala1796Glu
ENST00000586385.5:c.458C>A	ENSP00000465818.1:p.Ala153Glu
ENST00000591534.5:c.1001C>A	ENSP00000467329.1:p.Ala334Glu
ENST00000591849.5:c.227C>A	ENSP00000465347.1:p.Ala76Glu
NM_007294.3:c.5528C>A , LRG_292t1:c.5528C>A	NP_009225.1:p.Ala1843Glu
NM_007297.3:c.5387C>A	NP_009228.2:p.Ala1796Glu
NM_007298.3:c.2216C>A	NP_009229.2:p.Ala739Glu
NM_007299.3:c.*42C>A	NP_009230.2:n.*42C>A
NM_007300.3:c.5591C>A	NP_009231.2:p.Ala1864Glu
NR_027676.1:n.5664C>A
NM_007294.4:c.5528C>A MANE Select	NP_009225.1:p.Ala1843Glu
NM_007297.4:c.5387C>A	NP_009228.2:p.Ala1796Glu
NM_007299.4:c.*42C>A	NP_009230.2:n.*42C>A
NM_007300.4:c.5591C>A	NP_009231.2:p.Ala1864Glu
NR_027676.2:n.5705C>A