Canonical Allele Identifier: CA2082827906

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32376656_32376665delinsTTTTGTTTTC , CM000675.2:g.32376656_32376665delinsTTTTGTTTTC	GRCh38
NC_000013.10:g.32950793_32950802delinsTTTTGTTTTC , CM000675.1:g.32950793_32950802delinsTTTTGTTTTC	GRCh37
NC_000013.9:g.31848793_31848802delinsTTTTGTTTTC	NCBI36
NG_012772.3:g.66177_66186delinsTTTTGTTTTC , LRG_293:g.66177_66186delinsTTTTGTTTTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000470094.2:c.8633-14_8633-5delinsTTTTGTTTTC	ENSP00000434898.2:n.8633-14_8633-5delinsT...
ENST00000528762.2:c.8697-14_8697-5delinsTTTTGTTTTC	ENSP00000433168.2:n.8697-14_8697-5delinsT...
ENST00000530893.7:c.8264-14_8264-5delinsTTTTGTTTTC	ENSP00000499438.2:n.8264-14_8264-5delinsT...
ENST00000665585.2:c.*195-14_*195-5delinsTTTTGTTTTC	ENSP00000499570.2:n.*195-14_*195-5delinsT...
ENST00000666593.2:c.8633-14_8633-5delinsTTTTGTTTTC	ENSP00000499256.2:n.8633-14_8633-5delinsT...
ENST00000700202.2:c.8633-14_8633-5delinsTTTTGTTTTC	ENSP00000514856.2:n.8633-14_8633-5delinsT...
ENST00000700202.1:c.1100-14_1100-5delinsTTTTGTTTTC	ENSP00000514856.1:n.1100-14_1100-5delinsT...
ENST00000700203.1:n.746_755delinsTTTTGTTTTC
ENST00000380152.8:c.8633-14_8633-5delinsTTTTGTTTTC MANE Select	ENSP00000369497.3:n.8633-14_8633-5delinsT...
ENST00000544455.6:c.8633-14_8633-5delinsTTTTGTTTTC	ENSP00000439902.1:n.8633-14_8633-5delinsT...
ENST00000614259.2:c.8641-14_8641-5delinsTTTTGTTTTC	ENSP00000506251.1:n.8641-14_8641-5delinsT...
ENST00000665585.1:c.1511-14_1511-5delinsTTTTGTTTTC
ENST00000680887.1:c.8633-14_8633-5delinsTTTTGTTTTC	ENSP00000505508.1:n.8633-14_8633-5delinsT...
ENST00000380152.7:c.8633-14_8633-5delinsTTTTGTTTTC	ENSP00000369497.3:n.8633-14_8633-5delinsT...
ENST00000528762.1:c.195-14_195-5delinsTTTTGTTTTC	ENSP00000433168.1:n.195-14_195-5delinsTTT...
ENST00000544455.5:c.8633-14_8633-5delinsTTTTGTTTTC	ENSP00000439902.1:n.8633-14_8633-5delinsT...
NM_000059.3:c.8633-14_8633-5delinsTTTTGTTTTC , LRG_293t1:c.8633-14_8633-5delinsTTTTGTTTTC	NP_000050.2:n.8633-14_8633-5delinsTTTTGTT...
XM_011535203.1:c.8633-14_8633-5delinsTTTTGTTTTC	XP_011533505.1:n.8633-14_8633-5delinsTTTT...
XM_011535204.1:c.8537-14_8537-5delinsTTTTGTTTTC	XP_011533506.1:n.8537-14_8537-5delinsTTTT...
XM_011535205.1:c.8633-14_8633-5delinsTTTTGTTTTC	XP_011533507.1:n.8633-14_8633-5delinsTTTT...
NM_000059.4:c.8633-14_8633-5delinsTTTTGTTTTC MANE Select	NP_000050.3:n.8633-14_8633-5delinsTTTTGTT...