Canonical Allele Identifier: CA10591770

Gene: BRCA1

Linked Data

• MyVariant Identifiers: chr17:g.41223053A>C (hg19) ; chr17:g.43071036A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43071036A>C , CM000679.2:g.43071036A>C	GRCh38
NC_000017.10:g.41223053A>C , CM000679.1:g.41223053A>C	GRCh37
NC_000017.9:g.38476579A>C	NCBI36
NG_005905.2:g.146948T>G , LRG_292:g.146948T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461574.2:c.4875T>G	ENSP00000417241.2:p.Asn1625Lys
ENST00000470026.6:c.4878T>G	ENSP00000419274.2:p.Asn1626Lys
ENST00000473961.6:c.4752T>G	ENSP00000420201.2:p.Asn1584Lys
ENST00000476777.6:c.4872T>G	ENSP00000417554.2:p.Asn1624Lys
ENST00000477152.6:c.4800T>G	ENSP00000419988.2:p.Asn1600Lys
ENST00000478531.6:c.1566T>G	ENSP00000420412.2:p.Asn522Lys
ENST00000489037.2:c.4800T>G	ENSP00000420781.2:p.Asn1600Lys
ENST00000493919.6:c.1428T>G	ENSP00000418819.2:p.Asn476Lys
ENST00000494123.6:c.4878T>G	ENSP00000419103.2:p.Asn1626Lys
ENST00000497488.2:c.3990T>G	ENSP00000418986.2:p.Asn1330Lys
ENST00000618469.2:c.4878T>G	ENSP00000478114.2:p.Asn1626Lys
ENST00000634433.2:c.4755T>G	ENSP00000489431.2:p.Asn1585Lys
ENST00000644379.2:c.4944T>G	ENSP00000496570.2:p.Asn1648Lys
ENST00000644555.2:c.1428T>G	ENSP00000494614.2:p.Asn476Lys
ENST00000652672.2:c.4737T>G	ENSP00000498906.2:p.Asn1579Lys
ENST00000484087.6:c.1440T>G	ENSP00000419481.2:p.Asn480Lys
ENST00000700182.1:c.1485T>G	ENSP00000514849.1:p.Asn495Lys
ENST00000357654.9:c.4878T>G MANE Select	ENSP00000350283.3:p.Asn1626Lys
ENST00000471181.7:c.4941T>G	ENSP00000418960.2:p.Asn1647Lys
ENST00000644379.1:c.1265T>G
ENST00000352993.7:c.1452T>G	ENSP00000312236.5:p.Asn484Lys
ENST00000357654.7:c.4878T>G	ENSP00000350283.3:p.Asn1626Lys
ENST00000461221.5:c.*4661T>G	ENSP00000418548.1:n.*4661T>G
ENST00000468300.5:c.1566T>G	ENSP00000417148.1:p.Asn522Lys
ENST00000471181.6:c.4941T>G	ENSP00000418960.2:p.Asn1647Lys
ENST00000472490.1:n.31T>G
ENST00000478531.5:c.1566T>G	ENSP00000420412.1:p.Asn522Lys
ENST00000484087.5:c.1191T>G	ENSP00000419481.1:p.Asn397Lys
ENST00000491747.6:c.1566T>G	ENSP00000420705.2:p.Asn522Lys
ENST00000493795.5:c.4737T>G	ENSP00000418775.1:p.Asn1579Lys
ENST00000493919.5:c.1428T>G	ENSP00000418819.1:p.Asn476Lys
ENST00000586385.5:c.5-7085T>G	ENSP00000465818.1:n.5-7085T>G
ENST00000591534.5:c.351T>G	ENSP00000467329.1:p.Asn117Lys
ENST00000591849.5:c.-98-20846T>G	ENSP00000465347.1:n.-98-20846T>G
NM_007294.3:c.4878T>G , LRG_292t1:c.4878T>G	NP_009225.1:p.Asn1626Lys
NM_007297.3:c.4737T>G	NP_009228.2:p.Asn1579Lys
NM_007298.3:c.1566T>G	NP_009229.2:p.Asn522Lys
NM_007299.3:c.1566T>G	NP_009230.2:p.Asn522Lys
NM_007300.3:c.4941T>G	NP_009231.2:p.Asn1647Lys
NR_027676.1:n.5014T>G
NM_007294.4:c.4878T>G MANE Select	NP_009225.1:p.Asn1626Lys
NM_007297.4:c.4737T>G	NP_009228.2:p.Asn1579Lys
NM_007299.4:c.1566T>G	NP_009230.2:p.Asn522Lys
NM_007300.4:c.4941T>G	NP_009231.2:p.Asn1647Lys
NR_027676.2:n.5055T>G