Canonical Allele Identifier: CA983874003
Gene: BRCA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43067890_43067891insGAA , CM000679.2:g.43067890_43067891insGAA GRCh38
NC_000017.10:g.41219907_41219908insGAA , CM000679.1:g.41219907_41219908insGAA GRCh37
NC_000017.9:g.38473433_38473434insGAA NCBI36
NG_005905.2:g.150093_150094insTTC , LRG_292:g.150093_150094insTTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000461574.2:c.4984-196_4984-195insTTC ENSP00000417241.2:n.4984-196_4984-195insTTC
ENST00000470026.6:c.4987-196_4987-195insTTC ENSP00000419274.2:n.4987-196_4987-195insTTC
ENST00000473961.6:c.4861-196_4861-195insTTC ENSP00000420201.2:n.4861-196_4861-195insTTC
ENST00000476777.6:c.4981-196_4981-195insTTC ENSP00000417554.2:n.4981-196_4981-195insTTC
ENST00000477152.6:c.4909-196_4909-195insTTC ENSP00000419988.2:n.4909-196_4909-195insTTC
ENST00000478531.6:c.1675-196_1675-195insTTC ENSP00000420412.2:n.1675-196_1675-195insTTC
ENST00000489037.2:c.4909-196_4909-195insTTC ENSP00000420781.2:n.4909-196_4909-195insTTC
ENST00000493919.6:c.1537-196_1537-195insTTC ENSP00000418819.2:n.1537-196_1537-195insTTC
ENST00000494123.6:c.4987-196_4987-195insTTC ENSP00000419103.2:n.4987-196_4987-195insTTC
ENST00000497488.2:c.4099-196_4099-195insTTC ENSP00000418986.2:n.4099-196_4099-195insTTC
ENST00000618469.2:c.4987-196_4987-195insTTC ENSP00000478114.2:n.4987-196_4987-195insTTC
ENST00000634433.2:c.4864-196_4864-195insTTC ENSP00000489431.2:n.4864-196_4864-195insTTC
ENST00000644379.2:c.5053-196_5053-195insTTC ENSP00000496570.2:n.5053-196_5053-195insTTC
ENST00000644555.2:c.1537-196_1537-195insTTC ENSP00000494614.2:n.1537-196_1537-195insTTC
ENST00000652672.2:c.4846-196_4846-195insTTC ENSP00000498906.2:n.4846-196_4846-195insTTC
ENST00000484087.6:c.1549-196_1549-195insTTC ENSP00000419481.2:n.1549-196_1549-195insTTC
ENST00000357654.9:c.4987-196_4987-195insTTC MANE Select ENSP00000350283.3:n.4987-196_4987-195insTTC
ENST00000471181.7:c.5050-196_5050-195insTTC ENSP00000418960.2:n.5050-196_5050-195insTTC
ENST00000644379.1:c.1374-196_1374-195insTTC
ENST00000352993.7:c.1561-196_1561-195insTTC ENSP00000312236.5:n.1561-196_1561-195insTTC
ENST00000357654.7:c.4987-196_4987-195insTTC ENSP00000350283.3:n.4987-196_4987-195insTTC
ENST00000461221.5:c.*4770-196_*4770-195insTTC ENSP00000418548.1:n.*4770-196_*4770-195insTTC
ENST00000468300.5:c.1675-196_1675-195insTTC ENSP00000417148.1:n.1675-196_1675-195insTTC
ENST00000471181.6:c.5050-196_5050-195insTTC ENSP00000418960.2:n.5050-196_5050-195insTTC
ENST00000472490.1:n.140-196_140-195insTTC
ENST00000478531.5:c.1675-196_1675-195insTTC ENSP00000420412.1:n.1675-196_1675-195insTTC
ENST00000484087.5:c.1300-196_1300-195insTTC ENSP00000419481.1:n.1300-196_1300-195insTTC
ENST00000491747.6:c.1675-196_1675-195insTTC ENSP00000420705.2:n.1675-196_1675-195insTTC
ENST00000493795.5:c.4846-196_4846-195insTTC ENSP00000418775.1:n.4846-196_4846-195insTTC
ENST00000493919.5:c.1537-196_1537-195insTTC ENSP00000418819.1:n.1537-196_1537-195insTTC
ENST00000586385.5:c.5-3940_5-3939insTTC ENSP00000465818.1:n.5-3940_5-3939insTTC
ENST00000591534.5:c.460-196_460-195insTTC ENSP00000467329.1:n.460-196_460-195insTTC
ENST00000591849.5:c.-98-17701_-98-17700insTTC ENSP00000465347.1:n.-98-17701_-98-17700insTTC
NM_007294.3:c.4987-196_4987-195insTTC , LRG_292t1:c.4987-196_4987-195insTTC NP_009225.1:n.4987-196_4987-195insTTC
NM_007297.3:c.4846-196_4846-195insTTC NP_009228.2:n.4846-196_4846-195insTTC
NM_007298.3:c.1675-196_1675-195insTTC NP_009229.2:n.1675-196_1675-195insTTC
NM_007299.3:c.1675-196_1675-195insTTC NP_009230.2:n.1675-196_1675-195insTTC
NM_007300.3:c.5050-196_5050-195insTTC NP_009231.2:n.5050-196_5050-195insTTC
NR_027676.1:n.5123-196_5123-195insTTC
NM_007294.4:c.4987-196_4987-195insTTC MANE Select NP_009225.1:n.4987-196_4987-195insTTC
NM_007297.4:c.4846-196_4846-195insTTC NP_009228.2:n.4846-196_4846-195insTTC
NM_007299.4:c.1675-196_1675-195insTTC NP_009230.2:n.1675-196_1675-195insTTC
NM_007300.4:c.5050-196_5050-195insTTC NP_009231.2:n.5050-196_5050-195insTTC
NR_027676.2:n.5164-196_5164-195insTTC