Canonical Allele Identifier: CA2499224459

Gene: BRCA1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43091950_43091951insGGGT , CM000679.2:g.43091950_43091951insGGGT	GRCh38
NC_000017.10:g.41243967_41243968insGGGT , CM000679.1:g.41243967_41243968insGGGT	GRCh37
NC_000017.9:g.38497493_38497494insGGGT	NCBI36
NG_005905.2:g.126033_126034insACCC , LRG_292:g.126033_126034insACCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354071.8:n.3644_3645insACCC
ENST00000461574.2:c.3580_3581insACCC	ENSP00000417241.2:p.Thr1194AsnfsTer26
ENST00000470026.6:c.3580_3581insACCC	ENSP00000419274.2:p.Thr1194AsnfsTer26
ENST00000473961.6:c.3454_3455insACCC	ENSP00000420201.2:p.Thr1152AsnfsTer26
ENST00000476777.6:c.3577_3578insACCC	ENSP00000417554.2:p.Thr1193AsnfsTer26
ENST00000477152.6:c.3502_3503insACCC	ENSP00000419988.2:p.Thr1168AsnfsTer26
ENST00000478531.6:c.785-919_785-918insACCC	ENSP00000420412.2:n.785-919_785-918insACCC
ENST00000489037.2:c.3502_3503insACCC	ENSP00000420781.2:p.Thr1168AsnfsTer26
ENST00000493919.6:c.647-919_647-918insACCC	ENSP00000418819.2:n.647-919_647-918insACCC
ENST00000494123.6:c.3580_3581insACCC	ENSP00000419103.2:p.Thr1194AsnfsTer26
ENST00000497488.2:c.2692_2693insACCC	ENSP00000418986.2:p.Thr898AsnfsTer26
ENST00000618469.2:c.3580_3581insACCC	ENSP00000478114.2:p.Thr1194AsnfsTer26
ENST00000634433.2:c.3457_3458insACCC	ENSP00000489431.2:p.Thr1153AsnfsTer26
ENST00000644379.2:c.3580_3581insACCC	ENSP00000496570.2:p.Thr1194AsnfsTer26
ENST00000644555.2:c.647-919_647-918insACCC	ENSP00000494614.2:n.647-919_647-918insACCC
ENST00000652672.2:c.3439_3440insACCC	ENSP00000498906.2:p.Thr1147AsnfsTer26
ENST00000484087.6:c.665-919_665-918insACCC	ENSP00000419481.2:n.665-919_665-918insACCC
ENST00000700182.1:c.707-919_707-918insACCC	ENSP00000514849.1:n.707-919_707-918insACCC
ENST00000357654.9:c.3580_3581insACCC MANE Select	ENSP00000350283.3:p.Thr1194AsnfsTer26
ENST00000471181.7:c.3580_3581insACCC	ENSP00000418960.2:p.Thr1194AsnfsTer26
ENST00000352993.7:c.671-919_671-918insACCC	ENSP00000312236.5:n.671-919_671-918insACCC
ENST00000354071.7:c.3580_3581insACCC	ENSP00000326002.7:p.Thr1194AsnfsTer26
ENST00000357654.7:c.3580_3581insACCC	ENSP00000350283.3:p.Thr1194AsnfsTer26
ENST00000461221.5:c.*3363_*3364insACCC	ENSP00000418548.1:n.*3363_*3364insACCC
ENST00000468300.5:c.788-919_788-918insACCC	ENSP00000417148.1:n.788-919_788-918insACCC
ENST00000471181.6:c.3580_3581insACCC	ENSP00000418960.2:p.Thr1194AsnfsTer26
ENST00000478531.5:c.785-919_785-918insACCC	ENSP00000420412.1:n.785-919_785-918insACCC
ENST00000484087.5:c.410-919_410-918insACCC	ENSP00000419481.1:n.410-919_410-918insACCC
ENST00000487825.5:c.413-919_413-918insACCC	ENSP00000418212.1:n.413-919_413-918insACCC
ENST00000491747.6:c.788-919_788-918insACCC	ENSP00000420705.2:n.788-919_788-918insACCC
ENST00000493795.5:c.3439_3440insACCC	ENSP00000418775.1:p.Thr1147AsnfsTer26
ENST00000493919.5:c.647-919_647-918insACCC	ENSP00000418819.1:n.647-919_647-918insACCC
ENST00000586385.5:c.5-28000_5-27999insACCC	ENSP00000465818.1:n.5-28000_5-27999insACCC
ENST00000591534.5:c.-43-17430_-43-17429insACCC	ENSP00000467329.1:n.-43-17430_-43-17429insACCC
ENST00000591849.5:c.-99+33320_-99+33321insACCC	ENSP00000465347.1:n.-99+33320_-99+33321insACCC
NM_007294.3:c.3580_3581insACCC , LRG_292t1:c.3580_3581insACCC	NP_009225.1:p.Thr1194AsnfsTer26
NM_007297.3:c.3439_3440insACCC	NP_009228.2:p.Thr1147AsnfsTer26
NM_007298.3:c.788-919_788-918insACCC	NP_009229.2:n.788-919_788-918insACCC
NM_007299.3:c.788-919_788-918insACCC	NP_009230.2:n.788-919_788-918insACCC
NM_007300.3:c.3580_3581insACCC	NP_009231.2:p.Thr1194AsnfsTer26
NR_027676.1:n.3716_3717insACCC
NM_007294.4:c.3580_3581insACCC MANE Select	NP_009225.1:p.Thr1194AsnfsTer26
NM_007297.4:c.3439_3440insACCC	NP_009228.2:p.Thr1147AsnfsTer26
NM_007299.4:c.788-919_788-918insACCC	NP_009230.2:n.788-919_788-918insACCC
NM_007300.4:c.3580_3581insACCC	NP_009231.2:p.Thr1194AsnfsTer26
NR_027676.2:n.3757_3758insACCC