Canonical Allele Identifier: CA2622599500

Gene: BRCA2

Linked Data

• gnomAD v4: 13-32346890-C-CAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32346890_32346891insAAA , CM000675.2:g.32346890_32346891insAAA	GRCh38
NC_000013.10:g.32921027_32921028insAAA , CM000675.1:g.32921027_32921028insAAA	GRCh37
NC_000013.9:g.31819027_31819028insAAA	NCBI36
NG_012772.3:g.36411_36412insAAA , LRG_293:g.36411_36412insAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.7001_7002insAAA	ENSP00000434898.2:p.Pro2334_Phe2335insAsn
ENST00000528762.2:c.7001_7002insAAA	ENSP00000433168.2:p.Pro2334_Phe2335insAsn
ENST00000530893.7:c.6632_6633insAAA	ENSP00000499438.2:p.Pro2211_Phe2212insAsn
ENST00000665585.2:c.7001_7002insAAA	ENSP00000499570.2:p.Pro2334_Phe2335insAsn
ENST00000666593.2:c.7001_7002insAAA	ENSP00000499256.2:p.Pro2334_Phe2335insAsn
ENST00000700202.2:c.7001_7002insAAA	ENSP00000514856.2:p.Pro2334_Phe2335insAsn
ENST00000380152.8:c.7001_7002insAAA MANE Select	ENSP00000369497.3:p.Pro2334_Phe2335insAsn
ENST00000544455.6:c.7001_7002insAAA	ENSP00000439902.1:p.Pro2334_Phe2335insAsn
ENST00000614259.2:c.7001_7002insAAA	ENSP00000506251.1:p.Pro2334_Phe2335insAsn
ENST00000680887.1:c.7001_7002insAAA	ENSP00000505508.1:p.Pro2334_Phe2335insAsn
ENST00000380152.7:c.7001_7002insAAA	ENSP00000369497.3:p.Pro2334_Phe2335insAsn
ENST00000544455.5:c.7001_7002insAAA	ENSP00000439902.1:p.Pro2334_Phe2335insAsn
ENST00000614259.1:n.7001_7002insAAA
NM_000059.3:c.7001_7002insAAA , LRG_293t1:c.7001_7002insAAA	NP_000050.2:p.Pro2334_Phe2335insAsn
XM_011535203.1:c.7001_7002insAAA	XP_011533505.1:p.Pro2334_Phe2335insAsn
XM_011535204.1:c.6905_6906insAAA	XP_011533506.1:p.Pro2302_Phe2303insAsn
XM_011535205.1:c.7001_7002insAAA	XP_011533507.1:p.Pro2334_Phe2335insAsn
NM_000059.4:c.7001_7002insAAA MANE Select	NP_000050.3:p.Pro2334_Phe2335insAsn