Canonical Allele Identifier: CA10589621
Gene: BRCA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 266506

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43067611_43067698del , CM000679.2:g.43067611_43067698del GRCh38
NC_000017.10:g.41219628_41219715del , CM000679.1:g.41219628_41219715del GRCh37
NC_000017.9:g.38473154_38473241del NCBI36
NG_005905.2:g.150289_150376del , LRG_292:g.150289_150376del

Transcript Alleles

HGVS Amino-acid Change
ENST00000461574.2:c.4984_5071del
ENST00000470026.6:c.4987_5074del
ENST00000473961.6:c.4861_4948del
ENST00000476777.6:c.4981_5068del
ENST00000477152.6:c.4909_4996del
ENST00000478531.6:c.1675_1762del
ENST00000489037.2:c.4909_4996del
ENST00000493919.6:c.1537_1624del
ENST00000494123.6:c.4987_5074del
ENST00000497488.2:c.4099_4186del
ENST00000618469.2:c.4987_5074del
ENST00000634433.2:c.4864_4951del
ENST00000644379.2:c.5053_5140del
ENST00000644555.2:c.1537_1624del
ENST00000652672.2:c.4846_4933del
ENST00000484087.6:c.1549_1636del
ENST00000357654.9:c.4987_5074del
ENST00000471181.7:c.5050_5137del
ENST00000644379.1:c.1374_1461del
ENST00000352993.7:c.1561_1648del
ENST00000357654.7:c.4987_5074del
ENST00000461221.5:c.*4770_*4857del
ENST00000468300.5:c.1675_1762del
ENST00000471181.6:c.5050_5137del
ENST00000472490.1:n.140_227del
ENST00000478531.5:c.1675_1762del
ENST00000484087.5:c.1300_1387del
ENST00000491747.6:c.1675_1762del
ENST00000493795.5:c.4846_4933del
ENST00000493919.5:c.1537_1624del
ENST00000586385.5:c.5-3744_5-3657del ENSP00000465818.1:n.5-3744_5-3657del
ENST00000591534.5:c.460_547del
ENST00000591849.5:c.-98-17505_-98-17418del ENSP00000465347.1:n.-98-17505_-98-17418del
NM_007294.3:c.4987_5074del , LRG_292t1:c.4987_5074del
NM_007297.3:c.4846_4933del
NM_007298.3:c.1675_1762del
NM_007299.3:c.1675_1762del
NM_007300.3:c.5050_5137del
NR_027676.1:n.5123_5210del
NM_007294.4:c.4987_5074del
NM_007297.4:c.4846_4933del
NM_007299.4:c.1675_1762del
NM_007300.4:c.5050_5137del
NR_027676.2:n.5164_5251del