Canonical Allele Identifier: CA2260761995

Gene: BRCA1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43047666C= , CM000679.2:g.43047666C=	GRCh38
NC_000017.10:g.41199683C= , CM000679.1:g.41199683C=	GRCh37
NC_000017.9:g.38453209C=	NCBI36
NG_005905.2:g.170318G= , LRG_292:g.170318G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461574.2:c.5441G=	ENSP00000417241.2:p.Trp1814=
ENST00000470026.6:c.5444G=	ENSP00000419274.2:p.Trp1815=
ENST00000473961.6:c.5318G=	ENSP00000420201.2:p.Trp1773=
ENST00000476777.6:c.5438G=	ENSP00000417554.2:p.Trp1813=
ENST00000477152.6:c.5366G=	ENSP00000419988.2:p.Trp1789=
ENST00000478531.6:c.2132G=	ENSP00000420412.2:p.Trp711=
ENST00000489037.2:c.5366G=	ENSP00000420781.2:p.Trp1789=
ENST00000493919.6:c.1994G=	ENSP00000418819.2:p.Trp665=
ENST00000494123.6:c.5444G=	ENSP00000419103.2:p.Trp1815=
ENST00000497488.2:c.4556G=	ENSP00000418986.2:p.Trp1519=
ENST00000618469.2:c.5444G=	ENSP00000478114.2:p.Trp1815=
ENST00000634433.2:c.5321G=	ENSP00000489431.2:p.Trp1774=
ENST00000644379.2:c.5510G=	ENSP00000496570.2:p.Trp1837=
ENST00000644555.2:c.1994G=	ENSP00000494614.2:p.Trp665=
ENST00000652672.2:c.5303G=	ENSP00000498906.2:p.Trp1768=
ENST00000484087.6:c.2006G=	ENSP00000419481.2:p.Trp669=
ENST00000700081.1:n.1327G=
ENST00000700082.1:n.808G=
ENST00000357654.9:c.5444G= MANE Select	ENSP00000350283.3:p.Trp1815=
ENST00000471181.7:c.5507G=	ENSP00000418960.2:p.Trp1836=
ENST00000644379.1:c.1831G=
ENST00000352993.7:c.2018G=	ENSP00000312236.5:p.Trp673=
ENST00000357654.7:c.5444G=	ENSP00000350283.3:p.Trp1815=
ENST00000461221.5:c.*5227G=	ENSP00000418548.1:n.*5227G=
ENST00000468300.5:c.2058G=	ENSP00000417148.1:p.Leu686=
ENST00000471181.6:c.5507G=	ENSP00000418960.2:p.Trp1836=
ENST00000491747.6:c.2132G=	ENSP00000420705.2:p.Trp711=
ENST00000493795.5:c.5303G=	ENSP00000418775.1:p.Trp1768=
ENST00000586385.5:c.374G=	ENSP00000465818.1:p.Trp125=
ENST00000591534.5:c.917G=	ENSP00000467329.1:p.Trp306=
ENST00000591849.5:c.143G=	ENSP00000465347.1:p.Trp48=
NM_007294.3:c.5444G= , LRG_292t1:c.5444G=	NP_009225.1:p.Trp1815=
NM_007297.3:c.5303G=	NP_009228.2:p.Trp1768=
NM_007298.3:c.2132G=	NP_009229.2:p.Trp711=
NM_007299.3:c.2058G=	NP_009230.2:p.Leu686=
NM_007300.3:c.5507G=	NP_009231.2:p.Trp1836=
NR_027676.1:n.5580G=
NM_007294.4:c.5444G= MANE Select	NP_009225.1:p.Trp1815=
NM_007297.4:c.5303G=	NP_009228.2:p.Trp1768=
NM_007299.4:c.2058G=	NP_009230.2:p.Leu686=
NM_007300.4:c.5507G=	NP_009231.2:p.Trp1836=
NR_027676.2:n.5621G=