Canonical Allele Identifier: CA954689119

Gene: BRCA2

Linked Data

• gnomAD v3: 13-32318463-A-ATTTT
• gnomAD v4: 13-32318463-A-ATTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32318463_32318464insTTTT , CM000675.2:g.32318463_32318464insTTTT	GRCh38
NC_000013.10:g.32892600_32892601insTTTT , CM000675.1:g.32892600_32892601insTTTT	GRCh37
NC_000013.9:g.31790600_31790601insTTTT	NCBI36
NG_012772.3:g.7984_7985insTTTT , LRG_293:g.7984_7985insTTTT
NG_017006.2:g.1900_1901insAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.68-614_68-613insTTTT	ENSP00000434898.2:n.68-614_68-613insTTTT
ENST00000528762.2:c.68-614_68-613insTTTT	ENSP00000433168.2:n.68-614_68-613insTTTT
ENST00000530893.7:c.-302-614_-302-613insTTTT	ENSP00000499438.2:n.-302-614_-302-613insTTTT
ENST00000665585.2:c.68-614_68-613insTTTT	ENSP00000499570.2:n.68-614_68-613insTTTT
ENST00000666593.2:c.68-614_68-613insTTTT	ENSP00000499256.2:n.68-614_68-613insTTTT
ENST00000700202.2:c.68-614_68-613insTTTT	ENSP00000514856.2:n.68-614_68-613insTTTT
ENST00000700200.1:n.191+1936_191+1937insTTTT
ENST00000700201.1:c.68-614_68-613insTTTT	ENSP00000514855.1:n.68-614_68-613insTTTT
ENST00000380152.8:c.68-614_68-613insTTTT MANE Select	ENSP00000369497.3:n.68-614_68-613insTTTT
ENST00000544455.6:c.68-614_68-613insTTTT	ENSP00000439902.1:n.68-614_68-613insTTTT
ENST00000614259.2:c.68-614_68-613insTTTT	ENSP00000506251.1:n.68-614_68-613insTTTT
ENST00000680887.1:c.68-614_68-613insTTTT	ENSP00000505508.1:n.68-614_68-613insTTTT
ENST00000380152.7:c.68-614_68-613insTTTT	ENSP00000369497.3:n.68-614_68-613insTTTT
ENST00000530893.6:n.266-614_266-613insTTTT
ENST00000544455.5:c.68-614_68-613insTTTT	ENSP00000439902.1:n.68-614_68-613insTTTT
ENST00000614259.1:n.68-614_68-613insTTTT
NM_000059.3:c.68-614_68-613insTTTT , LRG_293t1:c.68-614_68-613insTTTT	NP_000050.2:n.68-614_68-613insTTTT
XM_011535203.1:c.68-614_68-613insTTTT	XP_011533505.1:n.68-614_68-613insTTTT
XM_011535204.1:c.68-614_68-613insTTTT	XP_011533506.1:n.68-614_68-613insTTTT
XM_011535205.1:c.68-614_68-613insTTTT	XP_011533507.1:n.68-614_68-613insTTTT
NM_000059.4:c.68-614_68-613insTTTT MANE Select	NP_000050.3:n.68-614_68-613insTTTT