Canonical Allele Identifier: CA915950126

Gene: BRCA1

Linked Data

• ClinVar Variation Id: 823774
• ClinVar RCV Id: RCV001020316 ; RCV001860981
• dbSNP Id: rs1597863644

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43092091_43092092del , CM000679.2:g.43092091_43092092del	GRCh38
NC_000017.10:g.41244108_41244109del , CM000679.1:g.41244108_41244109del	GRCh37
NC_000017.9:g.38497634_38497635del	NCBI36
NG_005905.2:g.125893_125894del , LRG_292:g.125893_125894del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354071.8:n.3504_3505del
ENST00000461574.2:c.3440_3441del	ENSP00000417241.2:p.Ser1147Ter
ENST00000470026.6:c.3440_3441del	ENSP00000419274.2:p.Ser1147Ter
ENST00000473961.6:c.3314_3315del	ENSP00000420201.2:p.Ser1105Ter
ENST00000476777.6:c.3437_3438del	ENSP00000417554.2:p.Ser1146Ter
ENST00000477152.6:c.3362_3363del	ENSP00000419988.2:p.Ser1121Ter
ENST00000478531.6:c.785-1059_785-1058del	ENSP00000420412.2:n.785-1059_785-1058del
ENST00000489037.2:c.3362_3363del	ENSP00000420781.2:p.Ser1121Ter
ENST00000493919.6:c.647-1059_647-1058del	ENSP00000418819.2:n.647-1059_647-1058del
ENST00000494123.6:c.3440_3441del	ENSP00000419103.2:p.Ser1147Ter
ENST00000497488.2:c.2552_2553del	ENSP00000418986.2:p.Ser851Ter
ENST00000618469.2:c.3440_3441del	ENSP00000478114.2:p.Ser1147Ter
ENST00000634433.2:c.3317_3318del	ENSP00000489431.2:p.Ser1106Ter
ENST00000644379.2:c.3440_3441del	ENSP00000496570.2:p.Ser1147Ter
ENST00000644555.2:c.647-1059_647-1058del	ENSP00000494614.2:n.647-1059_647-1058del
ENST00000652672.2:c.3299_3300del	ENSP00000498906.2:p.Ser1100Ter
ENST00000484087.6:c.665-1059_665-1058del	ENSP00000419481.2:n.665-1059_665-1058del
ENST00000700182.1:c.707-1059_707-1058del	ENSP00000514849.1:n.707-1059_707-1058del
ENST00000357654.9:c.3440_3441del MANE Select	ENSP00000350283.3:p.Ser1147Ter
ENST00000471181.7:c.3440_3441del	ENSP00000418960.2:p.Ser1147Ter
ENST00000352993.7:c.671-1059_671-1058del	ENSP00000312236.5:n.671-1059_671-1058del
ENST00000354071.7:c.3440_3441del	ENSP00000326002.7:p.Ser1147Ter
ENST00000357654.7:c.3440_3441del	ENSP00000350283.3:p.Ser1147Ter
ENST00000461221.5:c.*3223_*3224del	ENSP00000418548.1:n.*3223_*3224del
ENST00000468300.5:c.788-1059_788-1058del	ENSP00000417148.1:n.788-1059_788-1058del
ENST00000471181.6:c.3440_3441del	ENSP00000418960.2:p.Ser1147Ter
ENST00000478531.5:c.785-1059_785-1058del	ENSP00000420412.1:n.785-1059_785-1058del
ENST00000484087.5:c.410-1059_410-1058del	ENSP00000419481.1:n.410-1059_410-1058del
ENST00000487825.5:c.413-1059_413-1058del	ENSP00000418212.1:n.413-1059_413-1058del
ENST00000491747.6:c.788-1059_788-1058del	ENSP00000420705.2:n.788-1059_788-1058del
ENST00000493795.5:c.3299_3300del	ENSP00000418775.1:p.Ser1100Ter
ENST00000493919.5:c.647-1059_647-1058del	ENSP00000418819.1:n.647-1059_647-1058del
ENST00000586385.5:c.5-28140_5-28139del	ENSP00000465818.1:n.5-28140_5-28139del
ENST00000591534.5:c.-43-17570_-43-17569del	ENSP00000467329.1:n.-43-17570_-43-17569del
ENST00000591849.5:c.-99+33180_-99+33181del	ENSP00000465347.1:n.-99+33180_-99+33181del
NM_007294.3:c.3440_3441del , LRG_292t1:c.3440_3441del	NP_009225.1:p.Ser1147Ter
NM_007297.3:c.3299_3300del	NP_009228.2:p.Ser1100Ter
NM_007298.3:c.788-1059_788-1058del	NP_009229.2:n.788-1059_788-1058del
NM_007299.3:c.788-1059_788-1058del	NP_009230.2:n.788-1059_788-1058del
NM_007300.3:c.3440_3441del	NP_009231.2:p.Ser1147Ter
NR_027676.1:n.3576_3577del
NM_007294.4:c.3440_3441del MANE Select	NP_009225.1:p.Ser1147Ter
NM_007297.4:c.3299_3300del	NP_009228.2:p.Ser1100Ter
NM_007299.4:c.788-1059_788-1058del	NP_009230.2:n.788-1059_788-1058del
NM_007300.4:c.3440_3441del	NP_009231.2:p.Ser1147Ter
NR_027676.2:n.3617_3618del