Canonical Allele Identifier: CA954698115

Gene: BRCA2

Linked Data

• gnomAD v3: 13-32376512-ACCCTGTCT-A
• gnomAD v4: 13-32376512-ACCCTGTCT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32376514_32376521del , CM000675.2:g.32376514_32376521del	GRCh38
NC_000013.10:g.32950651_32950658del , CM000675.1:g.32950651_32950658del	GRCh37
NC_000013.9:g.31848651_31848658del	NCBI36
NG_012772.3:g.66035_66042del , LRG_293:g.66035_66042del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.8633-156_8633-149del	ENSP00000434898.2:n.8633-156_8633-149del
ENST00000528762.2:c.8697-156_8697-149del	ENSP00000433168.2:n.8697-156_8697-149del
ENST00000530893.7:c.8264-156_8264-149del	ENSP00000499438.2:n.8264-156_8264-149del
ENST00000665585.2:c.*195-156_*195-149del	ENSP00000499570.2:n.*195-156_*195-149del
ENST00000666593.2:c.8633-156_8633-149del	ENSP00000499256.2:n.8633-156_8633-149del
ENST00000700202.2:c.8633-156_8633-149del	ENSP00000514856.2:n.8633-156_8633-149del
ENST00000700202.1:c.1100-156_1100-149del	ENSP00000514856.1:n.1100-156_1100-149del
ENST00000700203.1:n.604_611del
ENST00000380152.8:c.8633-156_8633-149del MANE Select	ENSP00000369497.3:n.8633-156_8633-149del
ENST00000544455.6:c.8633-156_8633-149del	ENSP00000439902.1:n.8633-156_8633-149del
ENST00000614259.2:c.8641-156_8641-149del	ENSP00000506251.1:n.8641-156_8641-149del
ENST00000665585.1:c.1511-156_1511-149del
ENST00000680887.1:c.8633-156_8633-149del	ENSP00000505508.1:n.8633-156_8633-149del
ENST00000380152.7:c.8633-156_8633-149del	ENSP00000369497.3:n.8633-156_8633-149del
ENST00000528762.1:c.195-156_195-149del	ENSP00000433168.1:n.195-156_195-149del
ENST00000544455.5:c.8633-156_8633-149del	ENSP00000439902.1:n.8633-156_8633-149del
NM_000059.3:c.8633-156_8633-149del , LRG_293t1:c.8633-156_8633-149del	NP_000050.2:n.8633-156_8633-149del
XM_011535203.1:c.8633-156_8633-149del	XP_011533505.1:n.8633-156_8633-149del
XM_011535204.1:c.8537-156_8537-149del	XP_011533506.1:n.8537-156_8537-149del
XM_011535205.1:c.8633-156_8633-149del	XP_011533507.1:n.8633-156_8633-149del
NM_000059.4:c.8633-156_8633-149del MANE Select	NP_000050.3:n.8633-156_8633-149del