Canonical Allele Identifier: CA697355381

Gene: BRCA2

Linked Data

• dbSNP Id: rs1336985141
• gnomAD v3: 13-32362757-CTG-C
• gnomAD v4: 13-32362757-CTG-C
• MyVariant Identifiers: chr13:g.32936895_32936896del (hg19) ; chr13:g.32362758_32362759del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32362760_32362761del , CM000675.2:g.32362760_32362761del	GRCh38
NC_000013.10:g.32936897_32936898del , CM000675.1:g.32936897_32936898del	GRCh37
NC_000013.9:g.31834897_31834898del	NCBI36
NG_012772.3:g.52281_52282del , LRG_293:g.52281_52282del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.7976+67_7976+68del	ENSP00000434898.2:n.7976+67_7976+68del
ENST00000528762.2:c.7976+67_7976+68del	ENSP00000433168.2:n.7976+67_7976+68del
ENST00000530893.7:c.7607+67_7607+68del	ENSP00000499438.2:n.7607+67_7607+68del
ENST00000665585.2:c.7976+67_7976+68del	ENSP00000499570.2:n.7976+67_7976+68del
ENST00000666593.2:c.7976+67_7976+68del	ENSP00000499256.2:n.7976+67_7976+68del
ENST00000700202.2:c.7976+67_7976+68del	ENSP00000514856.2:n.7976+67_7976+68del
ENST00000700202.1:c.443+67_443+68del	ENSP00000514856.1:n.443+67_443+68del
ENST00000380152.8:c.7976+67_7976+68del MANE Select	ENSP00000369497.3:n.7976+67_7976+68del
ENST00000544455.6:c.7976+67_7976+68del	ENSP00000439902.1:n.7976+67_7976+68del
ENST00000614259.2:c.7984+67_7984+68del	ENSP00000506251.1:n.7984+67_7984+68del
ENST00000665585.1:c.541+67_541+68del
ENST00000680887.1:c.7976+67_7976+68del	ENSP00000505508.1:n.7976+67_7976+68del
ENST00000380152.7:c.7976+67_7976+68del	ENSP00000369497.3:n.7976+67_7976+68del
ENST00000544455.5:c.7976+67_7976+68del	ENSP00000439902.1:n.7976+67_7976+68del
NM_000059.3:c.7976+67_7976+68del , LRG_293t1:c.7976+67_7976+68del	NP_000050.2:n.7976+67_7976+68del
XM_011535203.1:c.7976+67_7976+68del	XP_011533505.1:n.7976+67_7976+68del
XM_011535204.1:c.7880+67_7880+68del	XP_011533506.1:n.7880+67_7880+68del
XM_011535205.1:c.7976+67_7976+68del	XP_011533507.1:n.7976+67_7976+68del
NM_000059.4:c.7976+67_7976+68del MANE Select	NP_000050.3:n.7976+67_7976+68del