Canonical Allele Identifier: CA2082751425
Gene: BRCA2 HGNC NCBI

Linked Data

dbSNP Id: rs2072347955

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32326395_32326396insTAG , CM000675.2:g.32326395_32326396insTAG GRCh38
NC_000013.10:g.32900532_32900533insTAG , CM000675.1:g.32900532_32900533insTAG GRCh37
NC_000013.9:g.31798532_31798533insTAG NCBI36
NG_012772.3:g.15916_15917insTAG , LRG_293:g.15916_15917insTAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.517-104_517-103insTAG ENSP00000434898.2:n.517-104_517-103insTAG
ENST00000528762.2:c.517-104_517-103insTAG ENSP00000433168.2:n.517-104_517-103insTAG
ENST00000530893.7:c.148-104_148-103insTAG ENSP00000499438.2:n.148-104_148-103insTAG
ENST00000665585.2:c.517-104_517-103insTAG ENSP00000499570.2:n.517-104_517-103insTAG
ENST00000666593.2:c.517-104_517-103insTAG ENSP00000499256.2:n.517-104_517-103insTAG
ENST00000700202.2:c.517-104_517-103insTAG ENSP00000514856.2:n.517-104_517-103insTAG
ENST00000700200.1:n.388-104_388-103insTAG
ENST00000700201.1:c.*296-104_*296-103insTAG ENSP00000514855.1:n.*296-104_*296-103insTAG
ENST00000380152.8:c.517-104_517-103insTAG MANE Select ENSP00000369497.3:n.517-104_517-103insTAG
ENST00000544455.6:c.517-104_517-103insTAG ENSP00000439902.1:n.517-104_517-103insTAG
ENST00000614259.2:c.517-104_517-103insTAG ENSP00000506251.1:n.517-104_517-103insTAG
ENST00000680887.1:c.517-104_517-103insTAG ENSP00000505508.1:n.517-104_517-103insTAG
ENST00000380152.7:c.517-104_517-103insTAG ENSP00000369497.3:n.517-104_517-103insTAG
ENST00000530893.6:n.715-104_715-103insTAG
ENST00000544455.5:c.517-104_517-103insTAG ENSP00000439902.1:n.517-104_517-103insTAG
ENST00000614259.1:n.517-104_517-103insTAG
NM_000059.3:c.517-104_517-103insTAG , LRG_293t1:c.517-104_517-103insTAG NP_000050.2:n.517-104_517-103insTAG
XM_011535203.1:c.517-104_517-103insTAG XP_011533505.1:n.517-104_517-103insTAG
XM_011535204.1:c.517-104_517-103insTAG XP_011533506.1:n.517-104_517-103insTAG
XM_011535205.1:c.517-104_517-103insTAG XP_011533507.1:n.517-104_517-103insTAG
NM_000059.4:c.517-104_517-103insTAG MANE Select NP_000050.3:n.517-104_517-103insTAG