Canonical Allele Identifier: CA2733909366

Gene: BRCA1

Linked Data

• dbSNP Id: rs2154166633

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43082674G>C , CM000679.2:g.43082674G>C	GRCh38
NC_000017.10:g.41234691G>C , CM000679.1:g.41234691G>C	GRCh37
NC_000017.9:g.38488217G>C	NCBI36
NG_005905.2:g.135310C>G , LRG_292:g.135310C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000461574.2:c.4186-99C>G	ENSP00000417241.2:n.4186-99C>G
ENST00000470026.6:c.4186-99C>G	ENSP00000419274.2:n.4186-99C>G
ENST00000473961.6:c.4060-99C>G	ENSP00000420201.2:n.4060-99C>G
ENST00000476777.6:c.4183-102C>G	ENSP00000417554.2:n.4183-102C>G
ENST00000477152.6:c.4108-99C>G	ENSP00000419988.2:n.4108-99C>G
ENST00000478531.6:c.874-99C>G	ENSP00000420412.2:n.874-99C>G
ENST00000489037.2:c.4108-99C>G	ENSP00000420781.2:n.4108-99C>G
ENST00000493919.6:c.736-99C>G	ENSP00000418819.2:n.736-99C>G
ENST00000494123.6:c.4186-99C>G	ENSP00000419103.2:n.4186-99C>G
ENST00000497488.2:c.3298-99C>G	ENSP00000418986.2:n.3298-99C>G
ENST00000618469.2:c.4186-99C>G	ENSP00000478114.2:n.4186-99C>G
ENST00000634433.2:c.4063-99C>G	ENSP00000489431.2:n.4063-99C>G
ENST00000644379.2:c.4186-99C>G	ENSP00000496570.2:n.4186-99C>G
ENST00000644555.2:c.736-99C>G	ENSP00000494614.2:n.736-99C>G
ENST00000652672.2:c.4045-99C>G	ENSP00000498906.2:n.4045-99C>G
ENST00000484087.6:c.754-102C>G	ENSP00000419481.2:n.754-102C>G
ENST00000700182.1:c.796-99C>G	ENSP00000514849.1:n.796-99C>G
ENST00000357654.9:c.4186-99C>G MANE Select	ENSP00000350283.3:n.4186-99C>G
ENST00000471181.7:c.4186-99C>G	ENSP00000418960.2:n.4186-99C>G
ENST00000644379.1:c.507-99C>G
ENST00000352993.7:c.760-99C>G	ENSP00000312236.5:n.760-99C>G
ENST00000357654.7:c.4186-99C>G	ENSP00000350283.3:n.4186-99C>G
ENST00000461221.5:c.*3969-99C>G	ENSP00000418548.1:n.*3969-99C>G
ENST00000461574.1:c.480-99C>G
ENST00000468300.5:c.877-99C>G	ENSP00000417148.1:n.877-99C>G
ENST00000471181.6:c.4186-99C>G	ENSP00000418960.2:n.4186-99C>G
ENST00000478531.5:c.874-99C>G	ENSP00000420412.1:n.874-99C>G
ENST00000484087.5:c.499-99C>G	ENSP00000419481.1:n.499-99C>G
ENST00000487825.5:c.502-99C>G	ENSP00000418212.1:n.502-99C>G
ENST00000491747.6:c.877-99C>G	ENSP00000420705.2:n.877-99C>G
ENST00000493795.5:c.4045-99C>G	ENSP00000418775.1:n.4045-99C>G
ENST00000493919.5:c.736-99C>G	ENSP00000418819.1:n.736-99C>G
ENST00000586385.5:c.5-18723C>G	ENSP00000465818.1:n.5-18723C>G
ENST00000591534.5:c.-43-8153C>G	ENSP00000467329.1:n.-43-8153C>G
ENST00000591849.5:c.-98-32484C>G	ENSP00000465347.1:n.-98-32484C>G
ENST00000621897.1:n.79+8C>G
NM_007294.3:c.4186-99C>G , LRG_292t1:c.4186-99C>G	NP_009225.1:n.4186-99C>G
NM_007297.3:c.4045-99C>G	NP_009228.2:n.4045-99C>G
NM_007298.3:c.877-99C>G	NP_009229.2:n.877-99C>G
NM_007299.3:c.877-99C>G	NP_009230.2:n.877-99C>G
NM_007300.3:c.4186-99C>G	NP_009231.2:n.4186-99C>G
NR_027676.1:n.4322-99C>G
NM_007294.4:c.4186-99C>G MANE Select	NP_009225.1:n.4186-99C>G
NM_007297.4:c.4045-99C>G	NP_009228.2:n.4045-99C>G
NM_007299.4:c.877-99C>G	NP_009230.2:n.877-99C>G
NM_007300.4:c.4186-99C>G	NP_009231.2:n.4186-99C>G
NR_027676.2:n.4363-99C>G