Canonical Allele Identifier: CA2260782339
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43091833T= , CM000679.2:g.43091833T= GRCh38
NC_000017.10:g.41243850T= , CM000679.1:g.41243850T= GRCh37
NC_000017.9:g.38497376T= NCBI36
NG_005905.2:g.126151A= , LRG_292:g.126151A=

Transcript Alleles

HGVS Amino-acid change
ENST00000354071.8:n.3762A=
ENST00000461574.2:c.3698A= ENSP00000417241.2:p.Lys1233=
ENST00000470026.6:c.3698A= ENSP00000419274.2:p.Lys1233=
ENST00000473961.6:c.3572A= ENSP00000420201.2:p.Lys1191=
ENST00000476777.6:c.3695A= ENSP00000417554.2:p.Lys1232=
ENST00000477152.6:c.3620A= ENSP00000419988.2:p.Lys1207=
ENST00000478531.6:c.785-801A= ENSP00000420412.2:n.785-801A=
ENST00000489037.2:c.3620A= ENSP00000420781.2:p.Lys1207=
ENST00000493919.6:c.647-801A= ENSP00000418819.2:n.647-801A=
ENST00000494123.6:c.3698A= ENSP00000419103.2:p.Lys1233=
ENST00000497488.2:c.2810A= ENSP00000418986.2:p.Lys937=
ENST00000618469.2:c.3698A= ENSP00000478114.2:p.Lys1233=
ENST00000634433.2:c.3575A= ENSP00000489431.2:p.Lys1192=
ENST00000644379.2:c.3698A= ENSP00000496570.2:p.Lys1233=
ENST00000644555.2:c.647-801A= ENSP00000494614.2:n.647-801A=
ENST00000652672.2:c.3557A= ENSP00000498906.2:p.Lys1186=
ENST00000484087.6:c.665-801A= ENSP00000419481.2:n.665-801A=
ENST00000700182.1:c.707-801A= ENSP00000514849.1:n.707-801A=
ENST00000357654.9:c.3698A= MANE Select ENSP00000350283.3:p.Lys1233=
ENST00000471181.7:c.3698A= ENSP00000418960.2:p.Lys1233=
ENST00000644379.1:c.19A=
ENST00000352993.7:c.671-801A= ENSP00000312236.5:n.671-801A=
ENST00000354071.7:c.3698A= ENSP00000326002.7:p.Lys1233=
ENST00000357654.7:c.3698A= ENSP00000350283.3:p.Lys1233=
ENST00000461221.5:c.*3481A= ENSP00000418548.1:n.*3481A=
ENST00000468300.5:c.788-801A= ENSP00000417148.1:n.788-801A=
ENST00000471181.6:c.3698A= ENSP00000418960.2:p.Lys1233=
ENST00000478531.5:c.785-801A= ENSP00000420412.1:n.785-801A=
ENST00000484087.5:c.410-801A= ENSP00000419481.1:n.410-801A=
ENST00000487825.5:c.413-801A= ENSP00000418212.1:n.413-801A=
ENST00000491747.6:c.788-801A= ENSP00000420705.2:n.788-801A=
ENST00000493795.5:c.3557A= ENSP00000418775.1:p.Lys1186=
ENST00000493919.5:c.647-801A= ENSP00000418819.1:n.647-801A=
ENST00000586385.5:c.5-27882A= ENSP00000465818.1:n.5-27882A=
ENST00000591534.5:c.-43-17312A= ENSP00000467329.1:n.-43-17312A=
ENST00000591849.5:c.-99+33438A= ENSP00000465347.1:n.-99+33438A=
NM_007294.3:c.3698A= , LRG_292t1:c.3698A= NP_009225.1:p.Lys1233=
NM_007297.3:c.3557A= NP_009228.2:p.Lys1186=
NM_007298.3:c.788-801A= NP_009229.2:n.788-801A=
NM_007299.3:c.788-801A= NP_009230.2:n.788-801A=
NM_007300.3:c.3698A= NP_009231.2:p.Lys1233=
NR_027676.1:n.3834A=
NM_007294.4:c.3698A= MANE Select NP_009225.1:p.Lys1233=
NM_007297.4:c.3557A= NP_009228.2:p.Lys1186=
NM_007299.4:c.788-801A= NP_009230.2:n.788-801A=
NM_007300.4:c.3698A= NP_009231.2:p.Lys1233=
NR_027676.2:n.3875A=