Canonical Allele Identifier: CA2622601204

Gene: BRCA2

Linked Data

• gnomAD v4: 13-32370657-G-GGCA

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32370657_32370658insGCA , CM000675.2:g.32370657_32370658insGCA	GRCh38
NC_000013.10:g.32944794_32944795insGCA , CM000675.1:g.32944794_32944795insGCA	GRCh37
NC_000013.9:g.31842794_31842795insGCA	NCBI36
NG_012772.3:g.60178_60179insGCA , LRG_293:g.60178_60179insGCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.8487+100_8487+101insGCA	ENSP00000434898.2:n.8487+100_8487+101insGCA
ENST00000528762.2:c.8487+100_8487+101insGCA	ENSP00000433168.2:n.8487+100_8487+101insGCA
ENST00000530893.7:c.8118+100_8118+101insGCA	ENSP00000499438.2:n.8118+100_8118+101insGCA
ENST00000665585.2:c.8487+100_8487+101insGCA	ENSP00000499570.2:n.8487+100_8487+101insGCA
ENST00000666593.2:c.8487+100_8487+101insGCA	ENSP00000499256.2:n.8487+100_8487+101insGCA
ENST00000700202.2:c.8487+100_8487+101insGCA	ENSP00000514856.2:n.8487+100_8487+101insGCA
ENST00000700202.1:c.954+100_954+101insGCA	ENSP00000514856.1:n.954+100_954+101insGCA
ENST00000380152.8:c.8487+100_8487+101insGCA MANE Select	ENSP00000369497.3:n.8487+100_8487+101insGCA
ENST00000544455.6:c.8487+100_8487+101insGCA	ENSP00000439902.1:n.8487+100_8487+101insGCA
ENST00000614259.2:c.8495+100_8495+101insGCA	ENSP00000506251.1:n.8495+100_8495+101insGCA
ENST00000665585.1:c.1052+100_1052+101insGCA
ENST00000680887.1:c.8487+100_8487+101insGCA	ENSP00000505508.1:n.8487+100_8487+101insGCA
ENST00000380152.7:c.8487+100_8487+101insGCA	ENSP00000369497.3:n.8487+100_8487+101insGCA
ENST00000544455.5:c.8487+100_8487+101insGCA	ENSP00000439902.1:n.8487+100_8487+101insGCA
NM_000059.3:c.8487+100_8487+101insGCA , LRG_293t1:c.8487+100_8487+101insGCA	NP_000050.2:n.8487+100_8487+101insGCA
XM_011535203.1:c.8487+100_8487+101insGCA	XP_011533505.1:n.8487+100_8487+101insGCA
XM_011535204.1:c.8391+100_8391+101insGCA	XP_011533506.1:n.8391+100_8391+101insGCA
XM_011535205.1:c.8487+100_8487+101insGCA	XP_011533507.1:n.8487+100_8487+101insGCA
NM_000059.4:c.8487+100_8487+101insGCA MANE Select	NP_000050.3:n.8487+100_8487+101insGCA