Canonical Allele Identifier: CA2260782027

Gene: BRCA1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43091548_43091549delinsGA , CM000679.2:g.43091548_43091549delinsGA	GRCh38
NC_000017.10:g.41243565_41243566delinsGA , CM000679.1:g.41243565_41243566delinsGA	GRCh37
NC_000017.9:g.38497091_38497092delinsGA	NCBI36
NG_005905.2:g.126435_126436delinsTC , LRG_292:g.126435_126436delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354071.8:n.4046_4047delinsTC
ENST00000461574.2:c.3982_3983delinsTC	ENSP00000417241.2:p.Ser1328=
ENST00000470026.6:c.3982_3983delinsTC	ENSP00000419274.2:p.Ser1328=
ENST00000473961.6:c.3856_3857delinsTC	ENSP00000420201.2:p.Ser1286=
ENST00000476777.6:c.3979_3980delinsTC	ENSP00000417554.2:p.Ser1327=
ENST00000477152.6:c.3904_3905delinsTC	ENSP00000419988.2:p.Ser1302=
ENST00000478531.6:c.785-517_785-516delinsTC	ENSP00000420412.2:n.785-517_785-516delinsTC
ENST00000489037.2:c.3904_3905delinsTC	ENSP00000420781.2:p.Ser1302=
ENST00000493919.6:c.647-517_647-516delinsTC	ENSP00000418819.2:n.647-517_647-516delinsTC
ENST00000494123.6:c.3982_3983delinsTC	ENSP00000419103.2:p.Ser1328=
ENST00000497488.2:c.3094_3095delinsTC	ENSP00000418986.2:p.Ser1032=
ENST00000618469.2:c.3982_3983delinsTC	ENSP00000478114.2:p.Ser1328=
ENST00000634433.2:c.3859_3860delinsTC	ENSP00000489431.2:p.Ser1287=
ENST00000644379.2:c.3982_3983delinsTC	ENSP00000496570.2:p.Ser1328=
ENST00000644555.2:c.647-517_647-516delinsTC	ENSP00000494614.2:n.647-517_647-516delinsTC
ENST00000652672.2:c.3841_3842delinsTC	ENSP00000498906.2:p.Ser1281=
ENST00000484087.6:c.665-517_665-516delinsTC	ENSP00000419481.2:n.665-517_665-516delinsTC
ENST00000700182.1:c.707-517_707-516delinsTC	ENSP00000514849.1:n.707-517_707-516delinsTC
ENST00000357654.9:c.3982_3983delinsTC MANE Select	ENSP00000350283.3:p.Ser1328=
ENST00000471181.7:c.3982_3983delinsTC	ENSP00000418960.2:p.Ser1328=
ENST00000644379.1:c.303_304delinsTC
ENST00000352993.7:c.671-517_671-516delinsTC	ENSP00000312236.5:n.671-517_671-516delinsTC
ENST00000354071.7:c.3982_3983delinsTC	ENSP00000326002.7:p.Ser1328=
ENST00000357654.7:c.3982_3983delinsTC	ENSP00000350283.3:p.Ser1328=
ENST00000461221.5:c.*3765_*3766delinsTC	ENSP00000418548.1:n.*3765_*3766delinsTC
ENST00000461574.1:c.276_277delinsTC
ENST00000468300.5:c.788-517_788-516delinsTC	ENSP00000417148.1:n.788-517_788-516delinsTC
ENST00000471181.6:c.3982_3983delinsTC	ENSP00000418960.2:p.Ser1328=
ENST00000478531.5:c.785-517_785-516delinsTC	ENSP00000420412.1:n.785-517_785-516delinsTC
ENST00000484087.5:c.410-517_410-516delinsTC	ENSP00000419481.1:n.410-517_410-516delinsTC
ENST00000487825.5:c.413-517_413-516delinsTC	ENSP00000418212.1:n.413-517_413-516delinsTC
ENST00000491747.6:c.788-517_788-516delinsTC	ENSP00000420705.2:n.788-517_788-516delinsTC
ENST00000493795.5:c.3841_3842delinsTC	ENSP00000418775.1:p.Ser1281=
ENST00000493919.5:c.647-517_647-516delinsTC	ENSP00000418819.1:n.647-517_647-516delinsTC
ENST00000586385.5:c.5-27598_5-27597delinsTC	ENSP00000465818.1:n.5-27598_5-27597delinsTC
ENST00000591534.5:c.-43-17028_-43-17027delinsTC	ENSP00000467329.1:n.-43-17028_-43-17027delinsTC
ENST00000591849.5:c.-99+33722_-99+33723delinsTC	ENSP00000465347.1:n.-99+33722_-99+33723delinsTC
NM_007294.3:c.3982_3983delinsTC , LRG_292t1:c.3982_3983delinsTC	NP_009225.1:p.Ser1328=
NM_007297.3:c.3841_3842delinsTC	NP_009228.2:p.Ser1281=
NM_007298.3:c.788-517_788-516delinsTC	NP_009229.2:n.788-517_788-516delinsTC
NM_007299.3:c.788-517_788-516delinsTC	NP_009230.2:n.788-517_788-516delinsTC
NM_007300.3:c.3982_3983delinsTC	NP_009231.2:p.Ser1328=
NR_027676.1:n.4118_4119delinsTC
NM_007294.4:c.3982_3983delinsTC MANE Select	NP_009225.1:p.Ser1328=
NM_007297.4:c.3841_3842delinsTC	NP_009228.2:p.Ser1281=
NM_007299.4:c.788-517_788-516delinsTC	NP_009230.2:n.788-517_788-516delinsTC
NM_007300.4:c.3982_3983delinsTC	NP_009231.2:p.Ser1328=
NR_027676.2:n.4159_4160delinsTC