Canonical Allele Identifier: CA10590699

Gene: BRCA1

Linked Data

• ClinVar Variation Id: 496395
• ClinVar RCV Id: RCV000588419 ; RCV001077304
• dbSNP Id: rs80357055
• MyVariant Identifiers: chr17:g.41201157G>A (hg19) ; chr17:g.43049140G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43049140G>A , CM000679.2:g.43049140G>A	GRCh38
NC_000017.10:g.41201157G>A , CM000679.1:g.41201157G>A	GRCh37
NC_000017.9:g.38454683G>A	NCBI36
NG_005905.2:g.168844C>T , LRG_292:g.168844C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461574.2:c.5384C>T	ENSP00000417241.2:p.Ser1795Leu
ENST00000470026.6:c.5387C>T	ENSP00000419274.2:p.Ser1796Leu
ENST00000473961.6:c.5261C>T	ENSP00000420201.2:p.Ser1754Leu
ENST00000476777.6:c.5381C>T	ENSP00000417554.2:p.Ser1794Leu
ENST00000477152.6:c.5309C>T	ENSP00000419988.2:p.Ser1770Leu
ENST00000478531.6:c.2075C>T	ENSP00000420412.2:p.Ser692Leu
ENST00000489037.2:c.5309C>T	ENSP00000420781.2:p.Ser1770Leu
ENST00000493919.6:c.1937C>T	ENSP00000418819.2:p.Ser646Leu
ENST00000494123.6:c.5387C>T	ENSP00000419103.2:p.Ser1796Leu
ENST00000497488.2:c.4499C>T	ENSP00000418986.2:p.Ser1500Leu
ENST00000618469.2:c.5387C>T	ENSP00000478114.2:p.Ser1796Leu
ENST00000634433.2:c.5264C>T	ENSP00000489431.2:p.Ser1755Leu
ENST00000644379.2:c.5453C>T	ENSP00000496570.2:p.Ser1818Leu
ENST00000644555.2:c.1937C>T	ENSP00000494614.2:p.Ser646Leu
ENST00000652672.2:c.5246C>T	ENSP00000498906.2:p.Ser1749Leu
ENST00000484087.6:c.1949C>T	ENSP00000419481.2:p.Ser650Leu
ENST00000700081.1:n.1270C>T
ENST00000357654.9:c.5387C>T MANE Select	ENSP00000350283.3:p.Ser1796Leu
ENST00000471181.7:c.5450C>T	ENSP00000418960.2:p.Ser1817Leu
ENST00000644379.1:c.1774C>T
ENST00000352993.7:c.1961C>T	ENSP00000312236.5:p.Ser654Leu
ENST00000357654.7:c.5387C>T	ENSP00000350283.3:p.Ser1796Leu
ENST00000461221.5:c.*5170C>T	ENSP00000418548.1:n.*5170C>T
ENST00000468300.5:c.2021-1437C>T	ENSP00000417148.1:n.2021-1437C>T
ENST00000471181.6:c.5450C>T	ENSP00000418960.2:p.Ser1817Leu
ENST00000491747.6:c.2075C>T	ENSP00000420705.2:p.Ser692Leu
ENST00000493795.5:c.5246C>T	ENSP00000418775.1:p.Ser1749Leu
ENST00000586385.5:c.317C>T	ENSP00000465818.1:p.Ser106Leu
ENST00000591534.5:c.860C>T	ENSP00000467329.1:p.Ser287Leu
ENST00000591849.5:c.86C>T	ENSP00000465347.1:p.Ser29Leu
NM_007294.3:c.5387C>T , LRG_292t1:c.5387C>T	NP_009225.1:p.Ser1796Leu
NM_007297.3:c.5246C>T	NP_009228.2:p.Ser1749Leu
NM_007298.3:c.2075C>T	NP_009229.2:p.Ser692Leu
NM_007299.3:c.2021-1437C>T	NP_009230.2:n.2021-1437C>T
NM_007300.3:c.5450C>T	NP_009231.2:p.Ser1817Leu
NR_027676.1:n.5523C>T
NM_007294.4:c.5387C>T MANE Select	NP_009225.1:p.Ser1796Leu
NM_007297.4:c.5246C>T	NP_009228.2:p.Ser1749Leu
NM_007299.4:c.2021-1437C>T	NP_009230.2:n.2021-1437C>T
NM_007300.4:c.5450C>T	NP_009231.2:p.Ser1817Leu
NR_027676.2:n.5564C>T