Canonical Allele Identifier: CA10593102

Gene: BRCA1

Linked Data

• MyVariant Identifiers: chr17:g.41234469A>C (hg19) ; chr17:g.43082452A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43082452A>C , CM000679.2:g.43082452A>C	GRCh38
NC_000017.10:g.41234469A>C , CM000679.1:g.41234469A>C	GRCh37
NC_000017.9:g.38487995A>C	NCBI36
NG_005905.2:g.135532T>G , LRG_292:g.135532T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000461574.2:c.4309T>G	ENSP00000417241.2:p.Ser1437Ala
ENST00000470026.6:c.4309T>G	ENSP00000419274.2:p.Ser1437Ala
ENST00000473961.6:c.4183T>G	ENSP00000420201.2:p.Ser1395Ala
ENST00000476777.6:c.4303T>G	ENSP00000417554.2:p.Ser1435Ala
ENST00000477152.6:c.4231T>G	ENSP00000419988.2:p.Ser1411Ala
ENST00000478531.6:c.997T>G	ENSP00000420412.2:p.Ser333Ala
ENST00000489037.2:c.4231T>G	ENSP00000420781.2:p.Ser1411Ala
ENST00000493919.6:c.859T>G	ENSP00000418819.2:p.Ser287Ala
ENST00000494123.6:c.4309T>G	ENSP00000419103.2:p.Ser1437Ala
ENST00000497488.2:c.3421T>G	ENSP00000418986.2:p.Ser1141Ala
ENST00000618469.2:c.4309T>G	ENSP00000478114.2:p.Ser1437Ala
ENST00000634433.2:c.4186T>G	ENSP00000489431.2:p.Ser1396Ala
ENST00000644379.2:c.4309T>G	ENSP00000496570.2:p.Ser1437Ala
ENST00000644555.2:c.859T>G	ENSP00000494614.2:p.Ser287Ala
ENST00000652672.2:c.4168T>G	ENSP00000498906.2:p.Ser1390Ala
ENST00000484087.6:c.874T>G	ENSP00000419481.2:p.Ser292Ala
ENST00000700182.1:c.919T>G	ENSP00000514849.1:p.Ser307Ala
ENST00000357654.9:c.4309T>G MANE Select	ENSP00000350283.3:p.Ser1437Ala
ENST00000471181.7:c.4309T>G	ENSP00000418960.2:p.Ser1437Ala
ENST00000644379.1:c.630T>G
ENST00000352993.7:c.883T>G	ENSP00000312236.5:p.Ser295Ala
ENST00000357654.7:c.4309T>G	ENSP00000350283.3:p.Ser1437Ala
ENST00000461221.5:c.*4092T>G	ENSP00000418548.1:n.*4092T>G
ENST00000461574.1:c.603T>G
ENST00000468300.5:c.1000T>G	ENSP00000417148.1:p.Ser334Ala
ENST00000471181.6:c.4309T>G	ENSP00000418960.2:p.Ser1437Ala
ENST00000478531.5:c.997T>G	ENSP00000420412.1:p.Ser333Ala
ENST00000484087.5:c.622T>G	ENSP00000419481.1:p.Ser208Ala
ENST00000487825.5:c.625T>G	ENSP00000418212.1:p.Ser209Ala
ENST00000491747.6:c.1000T>G	ENSP00000420705.2:p.Ser334Ala
ENST00000493795.5:c.4168T>G	ENSP00000418775.1:p.Ser1390Ala
ENST00000493919.5:c.859T>G	ENSP00000418819.1:p.Ser287Ala
ENST00000586385.5:c.5-18501T>G	ENSP00000465818.1:n.5-18501T>G
ENST00000591534.5:c.-43-7931T>G	ENSP00000467329.1:n.-43-7931T>G
ENST00000591849.5:c.-98-32262T>G	ENSP00000465347.1:n.-98-32262T>G
ENST00000621897.1:n.203T>G
NM_007294.3:c.4309T>G , LRG_292t1:c.4309T>G	NP_009225.1:p.Ser1437Ala
NM_007297.3:c.4168T>G	NP_009228.2:p.Ser1390Ala
NM_007298.3:c.1000T>G	NP_009229.2:p.Ser334Ala
NM_007299.3:c.1000T>G	NP_009230.2:p.Ser334Ala
NM_007300.3:c.4309T>G	NP_009231.2:p.Ser1437Ala
NR_027676.1:n.4445T>G
NM_007294.4:c.4309T>G MANE Select	NP_009225.1:p.Ser1437Ala
NM_007297.4:c.4168T>G	NP_009228.2:p.Ser1390Ala
NM_007299.4:c.1000T>G	NP_009230.2:p.Ser334Ala
NM_007300.4:c.4309T>G	NP_009231.2:p.Ser1437Ala
NR_027676.2:n.4486T>G