Canonical Allele Identifier: CA2260782511

Gene: BRCA1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43092004_43092007delinsACAG , CM000679.2:g.43092004_43092007delinsACAG	GRCh38
NC_000017.10:g.41244021_41244024delinsACAG , CM000679.1:g.41244021_41244024delinsACAG	GRCh37
NC_000017.9:g.38497547_38497550delinsACAG	NCBI36
NG_005905.2:g.125977_125980delinsCTGT , LRG_292:g.125977_125980delinsCTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354071.8:n.3588_3591delinsCTGT
ENST00000461574.2:c.3524_3527delinsCTGT	ENSP00000417241.2:p.Ala1175=
ENST00000470026.6:c.3524_3527delinsCTGT	ENSP00000419274.2:p.Ala1175=
ENST00000473961.6:c.3398_3401delinsCTGT	ENSP00000420201.2:p.Ala1133=
ENST00000476777.6:c.3521_3524delinsCTGT	ENSP00000417554.2:p.Ala1174=
ENST00000477152.6:c.3446_3449delinsCTGT	ENSP00000419988.2:p.Ala1149=
ENST00000478531.6:c.785-975_785-972delinsCTGT	ENSP00000420412.2:n.785-975_785-972delinsCTGT
ENST00000489037.2:c.3446_3449delinsCTGT	ENSP00000420781.2:p.Ala1149=
ENST00000493919.6:c.647-975_647-972delinsCTGT	ENSP00000418819.2:n.647-975_647-972delinsCTGT
ENST00000494123.6:c.3524_3527delinsCTGT	ENSP00000419103.2:p.Ala1175=
ENST00000497488.2:c.2636_2639delinsCTGT	ENSP00000418986.2:p.Ala879=
ENST00000618469.2:c.3524_3527delinsCTGT	ENSP00000478114.2:p.Ala1175=
ENST00000634433.2:c.3401_3404delinsCTGT	ENSP00000489431.2:p.Ala1134=
ENST00000644379.2:c.3524_3527delinsCTGT	ENSP00000496570.2:p.Ala1175=
ENST00000644555.2:c.647-975_647-972delinsCTGT	ENSP00000494614.2:n.647-975_647-972delinsCTGT
ENST00000652672.2:c.3383_3386delinsCTGT	ENSP00000498906.2:p.Ala1128=
ENST00000484087.6:c.665-975_665-972delinsCTGT	ENSP00000419481.2:n.665-975_665-972delinsCTGT
ENST00000700182.1:c.707-975_707-972delinsCTGT	ENSP00000514849.1:n.707-975_707-972delinsCTGT
ENST00000357654.9:c.3524_3527delinsCTGT MANE Select	ENSP00000350283.3:p.Ala1175=
ENST00000471181.7:c.3524_3527delinsCTGT	ENSP00000418960.2:p.Ala1175=
ENST00000352993.7:c.671-975_671-972delinsCTGT	ENSP00000312236.5:n.671-975_671-972delinsCTGT
ENST00000354071.7:c.3524_3527delinsCTGT	ENSP00000326002.7:p.Ala1175=
ENST00000357654.7:c.3524_3527delinsCTGT	ENSP00000350283.3:p.Ala1175=
ENST00000461221.5:c.*3307_*3310delinsCTGT	ENSP00000418548.1:n.*3307_*3310delinsCTGT
ENST00000468300.5:c.788-975_788-972delinsCTGT	ENSP00000417148.1:n.788-975_788-972delinsCTGT
ENST00000471181.6:c.3524_3527delinsCTGT	ENSP00000418960.2:p.Ala1175=
ENST00000478531.5:c.785-975_785-972delinsCTGT	ENSP00000420412.1:n.785-975_785-972delinsCTGT
ENST00000484087.5:c.410-975_410-972delinsCTGT	ENSP00000419481.1:n.410-975_410-972delinsCTGT
ENST00000487825.5:c.413-975_413-972delinsCTGT	ENSP00000418212.1:n.413-975_413-972delinsCTGT
ENST00000491747.6:c.788-975_788-972delinsCTGT	ENSP00000420705.2:n.788-975_788-972delinsCTGT
ENST00000493795.5:c.3383_3386delinsCTGT	ENSP00000418775.1:p.Ala1128=
ENST00000493919.5:c.647-975_647-972delinsCTGT	ENSP00000418819.1:n.647-975_647-972delinsCTGT
ENST00000586385.5:c.5-28056_5-28053delinsCTGT	ENSP00000465818.1:n.5-28056_5-28053delinsCTGT
ENST00000591534.5:c.-43-17486_-43-17483delinsCTGT	ENSP00000467329.1:n.-43-17486_-43-17483delinsCTGT
ENST00000591849.5:c.-99+33264_-99+33267delinsCTGT	ENSP00000465347.1:n.-99+33264_-99+33267delinsCTGT
NM_007294.3:c.3524_3527delinsCTGT , LRG_292t1:c.3524_3527delinsCTGT	NP_009225.1:p.Ala1175=
NM_007297.3:c.3383_3386delinsCTGT	NP_009228.2:p.Ala1128=
NM_007298.3:c.788-975_788-972delinsCTGT	NP_009229.2:n.788-975_788-972delinsCTGT
NM_007299.3:c.788-975_788-972delinsCTGT	NP_009230.2:n.788-975_788-972delinsCTGT
NM_007300.3:c.3524_3527delinsCTGT	NP_009231.2:p.Ala1175=
NR_027676.1:n.3660_3663delinsCTGT
NM_007294.4:c.3524_3527delinsCTGT MANE Select	NP_009225.1:p.Ala1175=
NM_007297.4:c.3383_3386delinsCTGT	NP_009228.2:p.Ala1128=
NM_007299.4:c.788-975_788-972delinsCTGT	NP_009230.2:n.788-975_788-972delinsCTGT
NM_007300.4:c.3524_3527delinsCTGT	NP_009231.2:p.Ala1175=
NR_027676.2:n.3701_3704delinsCTGT