Canonical Allele Identifier: CA647580018

Gene: BARD1

Linked Data

• COSMIC: COSN22332984

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214728597_214728598insA , CM000664.2:g.214728597_214728598insA	GRCh38
NC_000002.11:g.215593321_215593322insA , CM000664.1:g.215593321_215593322insA	GRCh37
NC_000002.10:g.215301566_215301567insA	NCBI36
NG_012047.2:g.86107_86108insT
NG_012047.3:g.86114_86115insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.*78_*79insT MANE Select	ENSP00000260947.4:n.*78_*79insT
ENST00000613374.5:c.*78_*79insT	ENSP00000484464.1:n.*78_*79insT
ENST00000613706.5:c.*78_*79insT	ENSP00000484976.2:n.*78_*79insT
ENST00000617164.5:c.*78_*79insT	ENSP00000480470.1:n.*78_*79insT
ENST00000619009.5:c.*78_*79insT	ENSP00000482293.1:n.*78_*79insT
ENST00000650978.1:c.3787_3788insT
ENST00000260947.8:c.*78_*79insT	ENSP00000260947.4:n.*78_*79insT
ENST00000432456.5:c.555_556insT
ENST00000471590.5:n.747_748insT
ENST00000613374.4:c.*78_*79insT	ENSP00000484464.1:n.*78_*79insT
ENST00000613706.4:c.*78_*79insT	ENSP00000484976.1:n.*78_*79insT
ENST00000617164.4:c.*78_*79insT	ENSP00000480470.1:n.*78_*79insT
ENST00000619009.4:c.*78_*79insT	ENSP00000482293.1:n.*78_*79insT
NM_000465.3:c.*78_*79insT	NP_000456.2:n.*78_*79insT
NM_001282543.1:c.*78_*79insT	NP_001269472.1:n.*78_*79insT
NM_001282545.1:c.*78_*79insT	NP_001269474.1:n.*78_*79insT
NM_001282548.1:c.*78_*79insT	NP_001269477.1:n.*78_*79insT
NM_001282549.1:c.*78_*79insT	NP_001269478.1:n.*78_*79insT
NR_104212.1:n.2405_2406insT
NR_104215.1:n.2348_2349insT
NR_104216.1:n.1604_1605insT
XM_011511567.1:c.*78_*79insT	XP_011509869.1:n.*78_*79insT
XM_017004613.1:c.*78_*79insT	XP_016860102.1:n.*78_*79insT
XR_002959322.1:n.2778_2779insT
NM_000465.4:c.*78_*79insT MANE Select	NP_000456.2:n.*78_*79insT
NM_001282543.2:c.*78_*79insT	NP_001269472.1:n.*78_*79insT
NM_001282545.2:c.*78_*79insT	NP_001269474.1:n.*78_*79insT
NM_001282548.2:c.*78_*79insT	NP_001269477.1:n.*78_*79insT
NM_001282549.2:c.*78_*79insT	NP_001269478.1:n.*78_*79insT
NR_104212.2:n.2377_2378insT
NR_104215.2:n.2320_2321insT
NR_104216.2:n.1576_1577insT