Canonical Allele Identifier: CA2565747995

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32376346_32376347insTG , CM000675.2:g.32376346_32376347insTG	GRCh38
NC_000013.10:g.32950483_32950484insTG , CM000675.1:g.32950483_32950484insTG	GRCh37
NC_000013.9:g.31848483_31848484insTG	NCBI36
NG_012772.3:g.65867_65868insTG , LRG_293:g.65867_65868insTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.8633-324_8633-323insTG	ENSP00000434898.2:n.8633-324_8633-323insTG
ENST00000528762.2:c.8697-324_8697-323insTG	ENSP00000433168.2:n.8697-324_8697-323insTG
ENST00000530893.7:c.8264-324_8264-323insTG	ENSP00000499438.2:n.8264-324_8264-323insTG
ENST00000665585.2:c.*195-324_*195-323insTG	ENSP00000499570.2:n.*195-324_*195-323insTG
ENST00000666593.2:c.8633-324_8633-323insTG	ENSP00000499256.2:n.8633-324_8633-323insTG
ENST00000700202.2:c.8633-324_8633-323insTG	ENSP00000514856.2:n.8633-324_8633-323insTG
ENST00000700202.1:c.1100-324_1100-323insTG	ENSP00000514856.1:n.1100-324_1100-323insTG
ENST00000700203.1:n.436_437insTG
ENST00000380152.8:c.8633-324_8633-323insTG MANE Select	ENSP00000369497.3:n.8633-324_8633-323insTG
ENST00000544455.6:c.8633-324_8633-323insTG	ENSP00000439902.1:n.8633-324_8633-323insTG
ENST00000614259.2:c.8641-324_8641-323insTG	ENSP00000506251.1:n.8641-324_8641-323insTG
ENST00000665585.1:c.1511-324_1511-323insTG
ENST00000680887.1:c.8633-324_8633-323insTG	ENSP00000505508.1:n.8633-324_8633-323insTG
ENST00000380152.7:c.8633-324_8633-323insTG	ENSP00000369497.3:n.8633-324_8633-323insTG
ENST00000528762.1:c.195-324_195-323insTG	ENSP00000433168.1:n.195-324_195-323insTG
ENST00000544455.5:c.8633-324_8633-323insTG	ENSP00000439902.1:n.8633-324_8633-323insTG
NM_000059.3:c.8633-324_8633-323insTG , LRG_293t1:c.8633-324_8633-323insTG	NP_000050.2:n.8633-324_8633-323insTG
XM_011535203.1:c.8633-324_8633-323insTG	XP_011533505.1:n.8633-324_8633-323insTG
XM_011535204.1:c.8537-324_8537-323insTG	XP_011533506.1:n.8537-324_8537-323insTG
XM_011535205.1:c.8633-324_8633-323insTG	XP_011533507.1:n.8633-324_8633-323insTG
NM_000059.4:c.8633-324_8633-323insTG MANE Select	NP_000050.3:n.8633-324_8633-323insTG