Canonical Allele Identifier: CA954700415
Gene: BRCA2 HGNC NCBI

Linked Data

dbSNP Id: rs2072750783

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32362906_32362907insTGCTTGCTTGCTTCCCTCTTTCCCCACCCCCTCCTT , CM000675.2:g.32362906_32362907insTGCTTGCTTGCTTCCCTCTTTCCCCACCCCCTCCTT GRCh38
NC_000013.10:g.32937043_32937044insTGCTTGCTTGCTTCCCTCTTTCCCCACCCCCTCCTT , CM000675.1:g.32937043_32937044insTGCTTGCTTGCTTCCCTCTTTCCCCACCCCCTCCTT GRCh37
NC_000013.9:g.31835043_31835044insTGCTTGCTTGCTTCCCTCTTTCCCCACCCCCTCCTT NCBI36
NG_012772.3:g.52427_52428insTGCTTGCTTGCTTCCCTCTTTCCCCACCCCCTCCTT , LRG_293:g.52427_52428insTGCTTGCTTGCTTCCCTCTTTCCCCACCCCCTCCTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.7976+213_7976+214insTGCTTGCTTGCTTCCCTCTTTCCCCACCCCCTCCTT ENSP00000434898.2:n.7976+213_7976+214insTGCTTGCTTGCTTCCCTCTTT...
ENST00000528762.2:c.7976+213_7976+214insTGCTTGCTTGCTTCCCTCTTTCCCCACCCCCTCCTT ENSP00000433168.2:n.7976+213_7976+214insTGCTTGCTTGCTTCCCTCTTT...
ENST00000530893.7:c.7607+213_7607+214insTGCTTGCTTGCTTCCCTCTTTCCCCACCCCCTCCTT ENSP00000499438.2:n.7607+213_7607+214insTGCTTGCTTGCTTCCCTCTTT...
ENST00000665585.2:c.7976+213_7976+214insTGCTTGCTTGCTTCCCTCTTTCCCCACCCCCTCCTT ENSP00000499570.2:n.7976+213_7976+214insTGCTTGCTTGCTTCCCTCTTT...
ENST00000666593.2:c.7976+213_7976+214insTGCTTGCTTGCTTCCCTCTTTCCCCACCCCCTCCTT ENSP00000499256.2:n.7976+213_7976+214insTGCTTGCTTGCTTCCCTCTTT...
ENST00000700202.2:c.7976+213_7976+214insTGCTTGCTTGCTTCCCTCTTTCCCCACCCCCTCCTT ENSP00000514856.2:n.7976+213_7976+214insTGCTTGCTTGCTTCCCTCTTT...
ENST00000700202.1:c.443+213_443+214insTGCTTGCTTGCTTCCCTCTTTCCCCACCCCCTCCTT ENSP00000514856.1:n.443+213_443+214insTGCTTGCTTGCTTCCCTCTTTCC...
ENST00000380152.8:c.7976+213_7976+214insTGCTTGCTTGCTTCCCTCTTTCCCCACCCCCTCCTT MANE Select ENSP00000369497.3:n.7976+213_7976+214insTGCTTGCTTGCTTCCCTCTTT...
ENST00000544455.6:c.7976+213_7976+214insTGCTTGCTTGCTTCCCTCTTTCCCCACCCCCTCCTT ENSP00000439902.1:n.7976+213_7976+214insTGCTTGCTTGCTTCCCTCTTT...
ENST00000614259.2:c.7984+213_7984+214insTGCTTGCTTGCTTCCCTCTTTCCCCACCCCCTCCTT ENSP00000506251.1:n.7984+213_7984+214insTGCTTGCTTGCTTCCCTCTTT...
ENST00000665585.1:c.541+213_541+214insTGCTTGCTTGCTTCCCTCTTTCCCCACCCCCTCCTT
ENST00000680887.1:c.7976+213_7976+214insTGCTTGCTTGCTTCCCTCTTTCCCCACCCCCTCCTT ENSP00000505508.1:n.7976+213_7976+214insTGCTTGCTTGCTTCCCTCTTT...
ENST00000380152.7:c.7976+213_7976+214insTGCTTGCTTGCTTCCCTCTTTCCCCACCCCCTCCTT ENSP00000369497.3:n.7976+213_7976+214insTGCTTGCTTGCTTCCCTCTTT...
ENST00000544455.5:c.7976+213_7976+214insTGCTTGCTTGCTTCCCTCTTTCCCCACCCCCTCCTT ENSP00000439902.1:n.7976+213_7976+214insTGCTTGCTTGCTTCCCTCTTT...
NM_000059.3:c.7976+213_7976+214insTGCTTGCTTGCTTCCCTCTTTCCCCACCCCCTCCTT , LRG_293t1:c.7976+213_7976+214insTGCTTGCTTGCTTCCCTCTTTCCCCACCCCCTCCTT NP_000050.2:n.7976+213_7976+214insTGCTTGCTTGCTTCCCTCTTTCCCCAC...
XM_011535203.1:c.7976+213_7976+214insTGCTTGCTTGCTTCCCTCTTTCCCCACCCCCTCCTT XP_011533505.1:n.7976+213_7976+214insTGCTTGCTTGCTTCCCTCTTTCCC...
XM_011535204.1:c.7880+213_7880+214insTGCTTGCTTGCTTCCCTCTTTCCCCACCCCCTCCTT XP_011533506.1:n.7880+213_7880+214insTGCTTGCTTGCTTCCCTCTTTCCC...
XM_011535205.1:c.7976+213_7976+214insTGCTTGCTTGCTTCCCTCTTTCCCCACCCCCTCCTT XP_011533507.1:n.7976+213_7976+214insTGCTTGCTTGCTTCCCTCTTTCCC...
NM_000059.4:c.7976+213_7976+214insTGCTTGCTTGCTTCCCTCTTTCCCCACCCCCTCCTT MANE Select NP_000050.3:n.7976+213_7976+214insTGCTTGCTTGCTTCCCTCTTTCCCCAC...