Canonical Allele Identifier: CA10593095

Gene: BRCA1

Linked Data

• dbSNP Id: rs2154149079
• MyVariant Identifiers: chr17:g.41234465G>T (hg19) ; chr17:g.43082448G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43082448G>T , CM000679.2:g.43082448G>T	GRCh38
NC_000017.10:g.41234465G>T , CM000679.1:g.41234465G>T	GRCh37
NC_000017.9:g.38487991G>T	NCBI36
NG_005905.2:g.135536C>A , LRG_292:g.135536C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000461574.2:c.4313C>A	ENSP00000417241.2:p.Ala1438Asp
ENST00000470026.6:c.4313C>A	ENSP00000419274.2:p.Ala1438Asp
ENST00000473961.6:c.4187C>A	ENSP00000420201.2:p.Ala1396Asp
ENST00000476777.6:c.4307C>A	ENSP00000417554.2:p.Ala1436Asp
ENST00000477152.6:c.4235C>A	ENSP00000419988.2:p.Ala1412Asp
ENST00000478531.6:c.1001C>A	ENSP00000420412.2:p.Ala334Asp
ENST00000489037.2:c.4235C>A	ENSP00000420781.2:p.Ala1412Asp
ENST00000493919.6:c.863C>A	ENSP00000418819.2:p.Ala288Asp
ENST00000494123.6:c.4313C>A	ENSP00000419103.2:p.Ala1438Asp
ENST00000497488.2:c.3425C>A	ENSP00000418986.2:p.Ala1142Asp
ENST00000618469.2:c.4313C>A	ENSP00000478114.2:p.Ala1438Asp
ENST00000634433.2:c.4190C>A	ENSP00000489431.2:p.Ala1397Asp
ENST00000644379.2:c.4313C>A	ENSP00000496570.2:p.Ala1438Asp
ENST00000644555.2:c.863C>A	ENSP00000494614.2:p.Ala288Asp
ENST00000652672.2:c.4172C>A	ENSP00000498906.2:p.Ala1391Asp
ENST00000484087.6:c.878C>A	ENSP00000419481.2:p.Ala293Asp
ENST00000700182.1:c.923C>A	ENSP00000514849.1:p.Ala308Asp
ENST00000357654.9:c.4313C>A MANE Select	ENSP00000350283.3:p.Ala1438Asp
ENST00000471181.7:c.4313C>A	ENSP00000418960.2:p.Ala1438Asp
ENST00000644379.1:c.634C>A
ENST00000352993.7:c.887C>A	ENSP00000312236.5:p.Ala296Asp
ENST00000357654.7:c.4313C>A	ENSP00000350283.3:p.Ala1438Asp
ENST00000461221.5:c.*4096C>A	ENSP00000418548.1:n.*4096C>A
ENST00000461574.1:c.607C>A
ENST00000468300.5:c.1004C>A	ENSP00000417148.1:p.Ala335Asp
ENST00000471181.6:c.4313C>A	ENSP00000418960.2:p.Ala1438Asp
ENST00000478531.5:c.1001C>A	ENSP00000420412.1:p.Ala334Asp
ENST00000484087.5:c.626C>A	ENSP00000419481.1:p.Ala209Asp
ENST00000487825.5:c.629C>A	ENSP00000418212.1:p.Ala210Asp
ENST00000491747.6:c.1004C>A	ENSP00000420705.2:p.Ala335Asp
ENST00000493795.5:c.4172C>A	ENSP00000418775.1:p.Ala1391Asp
ENST00000493919.5:c.863C>A	ENSP00000418819.1:p.Ala288Asp
ENST00000586385.5:c.5-18497C>A	ENSP00000465818.1:n.5-18497C>A
ENST00000591534.5:c.-43-7927C>A	ENSP00000467329.1:n.-43-7927C>A
ENST00000591849.5:c.-98-32258C>A	ENSP00000465347.1:n.-98-32258C>A
ENST00000621897.1:n.207C>A
NM_007294.3:c.4313C>A , LRG_292t1:c.4313C>A	NP_009225.1:p.Ala1438Asp
NM_007297.3:c.4172C>A	NP_009228.2:p.Ala1391Asp
NM_007298.3:c.1004C>A	NP_009229.2:p.Ala335Asp
NM_007299.3:c.1004C>A	NP_009230.2:p.Ala335Asp
NM_007300.3:c.4313C>A	NP_009231.2:p.Ala1438Asp
NR_027676.1:n.4449C>A
NM_007294.4:c.4313C>A MANE Select	NP_009225.1:p.Ala1438Asp
NM_007297.4:c.4172C>A	NP_009228.2:p.Ala1391Asp
NM_007299.4:c.1004C>A	NP_009230.2:p.Ala335Asp
NM_007300.4:c.4313C>A	NP_009231.2:p.Ala1438Asp
NR_027676.2:n.4490C>A