Canonical Allele Identifier: CA2082831407

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32362619_32362620delinsGG , CM000675.2:g.32362619_32362620delinsGG	GRCh38
NC_000013.10:g.32936756_32936757delinsGG , CM000675.1:g.32936756_32936757delinsGG	GRCh37
NC_000013.9:g.31834756_31834757delinsGG	NCBI36
NG_012772.3:g.52140_52141delinsGG , LRG_293:g.52140_52141delinsGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.7902_7903delinsGG	ENSP00000434898.2:p.Met2634=
ENST00000528762.2:c.7902_7903delinsGG	ENSP00000433168.2:p.Met2634=
ENST00000530893.7:c.7533_7534delinsGG	ENSP00000499438.2:p.Met2511=
ENST00000665585.2:c.7902_7903delinsGG	ENSP00000499570.2:p.Met2634=
ENST00000666593.2:c.7902_7903delinsGG	ENSP00000499256.2:p.Met2634=
ENST00000700202.2:c.7902_7903delinsGG	ENSP00000514856.2:p.Met2634=
ENST00000700202.1:c.369_370delinsGG	ENSP00000514856.1:p.Met123=
ENST00000380152.8:c.7902_7903delinsGG MANE Select	ENSP00000369497.3:p.Met2634=
ENST00000544455.6:c.7902_7903delinsGG	ENSP00000439902.1:p.Met2634=
ENST00000614259.2:c.7910_7911delinsGG	ENSP00000506251.1:p.Trp2637=
ENST00000665585.1:c.467_468delinsGG
ENST00000680887.1:c.7902_7903delinsGG	ENSP00000505508.1:p.Met2634=
ENST00000380152.7:c.7902_7903delinsGG	ENSP00000369497.3:p.Met2634=
ENST00000544455.5:c.7902_7903delinsGG	ENSP00000439902.1:p.Met2634=
ENST00000614259.1:n.7910_7911delinsGG
NM_000059.3:c.7902_7903delinsGG , LRG_293t1:c.7902_7903delinsGG	NP_000050.2:p.Met2634=
XM_011535203.1:c.7902_7903delinsGG	XP_011533505.1:p.Met2634=
XM_011535204.1:c.7806_7807delinsGG	XP_011533506.1:p.Met2602=
XM_011535205.1:c.7902_7903delinsGG	XP_011533507.1:p.Met2634=
NM_000059.4:c.7902_7903delinsGG MANE Select	NP_000050.3:p.Met2634=