Canonical Allele Identifier: CA2622601330
Gene: BRCA2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32371170_32371171insC , CM000675.2:g.32371170_32371171insC GRCh38
NC_000013.10:g.32945307_32945308insC , CM000675.1:g.32945307_32945308insC GRCh37
NC_000013.9:g.31843307_31843308insC NCBI36
NG_012772.3:g.60691_60692insC , LRG_293:g.60691_60692insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.8632+70_8632+71insC ENSP00000434898.2:n.8632+70_8632+71insC
ENST00000528762.2:c.8632+70_8632+71insC ENSP00000433168.2:n.8632+70_8632+71insC
ENST00000530893.7:c.8263+70_8263+71insC ENSP00000499438.2:n.8263+70_8263+71insC
ENST00000665585.2:c.8632+70_8632+71insC ENSP00000499570.2:n.8632+70_8632+71insC
ENST00000666593.2:c.8632+70_8632+71insC ENSP00000499256.2:n.8632+70_8632+71insC
ENST00000700202.2:c.8632+70_8632+71insC ENSP00000514856.2:n.8632+70_8632+71insC
ENST00000700202.1:c.1099+70_1099+71insC ENSP00000514856.1:n.1099+70_1099+71insC
ENST00000380152.8:c.8632+70_8632+71insC MANE Select ENSP00000369497.3:n.8632+70_8632+71insC
ENST00000544455.6:c.8632+70_8632+71insC ENSP00000439902.1:n.8632+70_8632+71insC
ENST00000614259.2:c.8640+70_8640+71insC ENSP00000506251.1:n.8640+70_8640+71insC
ENST00000665585.1:c.1197+70_1197+71insC
ENST00000680887.1:c.8632+70_8632+71insC ENSP00000505508.1:n.8632+70_8632+71insC
ENST00000380152.7:c.8632+70_8632+71insC ENSP00000369497.3:n.8632+70_8632+71insC
ENST00000528762.1:c.130+70_130+71insC ENSP00000433168.1:n.130+70_130+71insC
ENST00000544455.5:c.8632+70_8632+71insC ENSP00000439902.1:n.8632+70_8632+71insC
NM_000059.3:c.8632+70_8632+71insC , LRG_293t1:c.8632+70_8632+71insC NP_000050.2:n.8632+70_8632+71insC
XM_011535203.1:c.8632+70_8632+71insC XP_011533505.1:n.8632+70_8632+71insC
XM_011535204.1:c.8536+70_8536+71insC XP_011533506.1:n.8536+70_8536+71insC
XM_011535205.1:c.8632+70_8632+71insC XP_011533507.1:n.8632+70_8632+71insC
NM_000059.4:c.8632+70_8632+71insC MANE Select NP_000050.3:n.8632+70_8632+71insC