Canonical Allele Identifier: CA2622601702

Gene: BRCA2

Linked Data

• gnomAD v4: 13-32376919-T-TCC

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32376919_32376920insCC , CM000675.2:g.32376919_32376920insCC	GRCh38
NC_000013.10:g.32951056_32951057insCC , CM000675.1:g.32951056_32951057insCC	GRCh37
NC_000013.9:g.31849056_31849057insCC	NCBI36
NG_012772.3:g.66440_66441insCC , LRG_293:g.66440_66441insCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.8754+128_8754+129insCC	ENSP00000434898.2:n.8754+128_8754+129insCC
ENST00000528762.2:c.*121+128_*121+129insCC	ENSP00000433168.2:n.*121+128_*121+129insCC
ENST00000530893.7:c.8385+128_8385+129insCC	ENSP00000499438.2:n.8385+128_8385+129insCC
ENST00000665585.2:c.*316+128_*316+129insCC	ENSP00000499570.2:n.*316+128_*316+129insCC
ENST00000666593.2:c.8754+128_8754+129insCC	ENSP00000499256.2:n.8754+128_8754+129insCC
ENST00000700202.2:c.8754+128_8754+129insCC	ENSP00000514856.2:n.8754+128_8754+129insCC
ENST00000700202.1:c.1221+128_1221+129insCC	ENSP00000514856.1:n.1221+128_1221+129insCC
ENST00000700203.1:n.881+128_881+129insCC
ENST00000380152.8:c.8754+128_8754+129insCC MANE Select	ENSP00000369497.3:n.8754+128_8754+129insCC
ENST00000544455.6:c.8754+128_8754+129insCC	ENSP00000439902.1:n.8754+128_8754+129insCC
ENST00000614259.2:c.8762+128_8762+129insCC	ENSP00000506251.1:n.8762+128_8762+129insCC
ENST00000665585.1:c.1632+128_1632+129insCC
ENST00000680887.1:c.8754+128_8754+129insCC	ENSP00000505508.1:n.8754+128_8754+129insCC
ENST00000380152.7:c.8754+128_8754+129insCC	ENSP00000369497.3:n.8754+128_8754+129insCC
ENST00000528762.1:c.316+128_316+129insCC	ENSP00000433168.1:n.316+128_316+129insCC
ENST00000544455.5:c.8754+128_8754+129insCC	ENSP00000439902.1:n.8754+128_8754+129insCC
NM_000059.3:c.8754+128_8754+129insCC , LRG_293t1:c.8754+128_8754+129insCC	NP_000050.2:n.8754+128_8754+129insCC
XM_011535203.1:c.8754+128_8754+129insCC	XP_011533505.1:n.8754+128_8754+129insCC
XM_011535204.1:c.8658+128_8658+129insCC	XP_011533506.1:n.8658+128_8658+129insCC
XM_011535205.1:c.8754+128_8754+129insCC	XP_011533507.1:n.8754+128_8754+129insCC
NM_000059.4:c.8754+128_8754+129insCC MANE Select	NP_000050.3:n.8754+128_8754+129insCC