Canonical Allele Identifier: CA954697779

Gene: BRCA2

Linked Data

• gnomAD v3: 13-32376198-C-CTTTT
• gnomAD v4: 13-32376198-C-CTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32376198_32376199insTTTT , CM000675.2:g.32376198_32376199insTTTT	GRCh38
NC_000013.10:g.32950335_32950336insTTTT , CM000675.1:g.32950335_32950336insTTTT	GRCh37
NC_000013.9:g.31848335_31848336insTTTT	NCBI36
NG_012772.3:g.65719_65720insTTTT , LRG_293:g.65719_65720insTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.8633-472_8633-471insTTTT	ENSP00000434898.2:n.8633-472_8633-471insTTTT
ENST00000528762.2:c.8697-472_8697-471insTTTT	ENSP00000433168.2:n.8697-472_8697-471insTTTT
ENST00000530893.7:c.8264-472_8264-471insTTTT	ENSP00000499438.2:n.8264-472_8264-471insTTTT
ENST00000665585.2:c.*195-472_*195-471insTTTT	ENSP00000499570.2:n.*195-472_*195-471insTTTT
ENST00000666593.2:c.8633-472_8633-471insTTTT	ENSP00000499256.2:n.8633-472_8633-471insTTTT
ENST00000700202.2:c.8633-472_8633-471insTTTT	ENSP00000514856.2:n.8633-472_8633-471insTTTT
ENST00000700202.1:c.1100-472_1100-471insTTTT	ENSP00000514856.1:n.1100-472_1100-471insTTTT
ENST00000700203.1:n.288_289insTTTT
ENST00000380152.8:c.8633-472_8633-471insTTTT MANE Select	ENSP00000369497.3:n.8633-472_8633-471insTTTT
ENST00000544455.6:c.8633-472_8633-471insTTTT	ENSP00000439902.1:n.8633-472_8633-471insTTTT
ENST00000614259.2:c.8641-472_8641-471insTTTT	ENSP00000506251.1:n.8641-472_8641-471insTTTT
ENST00000665585.1:c.1511-472_1511-471insTTTT
ENST00000680887.1:c.8633-472_8633-471insTTTT	ENSP00000505508.1:n.8633-472_8633-471insTTTT
ENST00000380152.7:c.8633-472_8633-471insTTTT	ENSP00000369497.3:n.8633-472_8633-471insTTTT
ENST00000528762.1:c.195-472_195-471insTTTT	ENSP00000433168.1:n.195-472_195-471insTTTT
ENST00000544455.5:c.8633-472_8633-471insTTTT	ENSP00000439902.1:n.8633-472_8633-471insTTTT
NM_000059.3:c.8633-472_8633-471insTTTT , LRG_293t1:c.8633-472_8633-471insTTTT	NP_000050.2:n.8633-472_8633-471insTTTT
XM_011535203.1:c.8633-472_8633-471insTTTT	XP_011533505.1:n.8633-472_8633-471insTTTT
XM_011535204.1:c.8537-472_8537-471insTTTT	XP_011533506.1:n.8537-472_8537-471insTTTT
XM_011535205.1:c.8633-472_8633-471insTTTT	XP_011533507.1:n.8633-472_8633-471insTTTT
NM_000059.4:c.8633-472_8633-471insTTTT MANE Select	NP_000050.3:n.8633-472_8633-471insTTTT