Canonical Allele Identifier: CA2082749723

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32326101_32326102delinsTC , CM000675.2:g.32326101_32326102delinsTC	GRCh38
NC_000013.10:g.32900238_32900239delinsTC , CM000675.1:g.32900238_32900239delinsTC	GRCh37
NC_000013.9:g.31798238_31798239delinsTC	NCBI36
NG_012772.3:g.15622_15623delinsTC , LRG_293:g.15622_15623delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.426_427delinsTC	ENSP00000434898.2:p.Ser142=
ENST00000528762.2:c.426_427delinsTC	ENSP00000433168.2:p.Ser142=
ENST00000530893.7:c.57_58delinsTC	ENSP00000499438.2:p.Ser19=
ENST00000665585.2:c.426_427delinsTC	ENSP00000499570.2:p.Ser142=
ENST00000666593.2:c.426_427delinsTC	ENSP00000499256.2:p.Ser142=
ENST00000700202.2:c.426_427delinsTC	ENSP00000514856.2:p.Ser142=
ENST00000700200.1:n.297_298delinsTC
ENST00000700201.1:c.*205_*206delinsTC	ENSP00000514855.1:n.*205_*206delinsTC
ENST00000380152.8:c.426_427delinsTC MANE Select	ENSP00000369497.3:p.Ser142=
ENST00000544455.6:c.426_427delinsTC	ENSP00000439902.1:p.Ser142=
ENST00000614259.2:c.426_427delinsTC	ENSP00000506251.1:p.Ser142=
ENST00000680887.1:c.426_427delinsTC	ENSP00000505508.1:p.Ser142=
ENST00000380152.7:c.426_427delinsTC	ENSP00000369497.3:p.Ser142=
ENST00000530893.6:n.624_625delinsTC
ENST00000544455.5:c.426_427delinsTC	ENSP00000439902.1:p.Ser142=
ENST00000614259.1:n.426_427delinsTC
NM_000059.3:c.426_427delinsTC , LRG_293t1:c.426_427delinsTC	NP_000050.2:p.Ser142=
XM_011535203.1:c.426_427delinsTC	XP_011533505.1:p.Ser142=
XM_011535204.1:c.426_427delinsTC	XP_011533506.1:p.Ser142=
XM_011535205.1:c.426_427delinsTC	XP_011533507.1:p.Ser142=
NM_000059.4:c.426_427delinsTC MANE Select	NP_000050.3:p.Ser142=