Canonical Allele Identifier: CA387761078

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32394779C>T , CM000675.2:g.32394779C>T	GRCh38
NC_000013.10:g.32968916C>T , CM000675.1:g.32968916C>T	GRCh37
NC_000013.9:g.31866916C>T	NCBI36
NG_012772.3:g.84300C>T , LRG_293:g.84300C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000059.4:c.9347C>T MANE Select	NP_000050.3:p.Pro3116Leu
ENST00000380152.8:c.9347C>T MANE Select	ENSP00000369497.3:p.Pro3116Leu
NM_000059.3:c.9347C>T , LRG_293t1:c.9347C>T	NP_000050.2:p.Pro3116Leu
ENST00000380152.7:c.9347C>T	ENSP00000369497.3:p.Pro3116Leu
ENST00000470094.1:c.304C>T
ENST00000470094.2:c.9347C>T	ENSP00000434898.2:p.Pro3116Leu
ENST00000528762.2:c.*714C>T	ENSP00000433168.2:n.*714C>T
ENST00000530893.7:c.8978C>T	ENSP00000499438.2:p.Pro2993Leu
ENST00000544455.5:c.9347C>T	ENSP00000439902.1:p.Pro3116Leu
ENST00000544455.6:c.9347C>T	ENSP00000439902.1:p.Pro3116Leu
ENST00000614259.2:c.9355C>T	ENSP00000506251.1:n.9355C>T
ENST00000665585.1:c.2225C>T
ENST00000665585.2:c.*909C>T	ENSP00000499570.2:n.*909C>T
ENST00000666593.1:c.369C>T	ENSP00000499256.1:n.369C>T
ENST00000666593.2:c.*192C>T	ENSP00000499256.2:n.*192C>T
ENST00000680887.1:c.9347C>T	ENSP00000505508.1:p.Pro3116Leu
ENST00000700202.1:c.1763C>T	ENSP00000514856.1:p.Pro588Leu
ENST00000700202.2:c.9296C>T	ENSP00000514856.2:p.Pro3099Leu
ENST00000700203.1:n.1474C>T
XM_011535203.1:c.9347C>T	XP_011533505.1:p.Pro3116Leu
XM_011535204.1:c.9251C>T	XP_011533506.1:p.Pro3084Leu