Canonical Allele Identifier: CA647580019

Gene: BARD1

Linked Data

• COSMIC: COSN20467111

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214728638_214728639insA , CM000664.2:g.214728638_214728639insA	GRCh38
NC_000002.11:g.215593362_215593363insA , CM000664.1:g.215593362_215593363insA	GRCh37
NC_000002.10:g.215301607_215301608insA	NCBI36
NG_012047.2:g.86066_86067insT
NG_012047.3:g.86073_86074insT

Transcript Alleles

HGVS	Amino-acid change
ENST00000260947.9:c.*37_*38insT MANE Select	ENSP00000260947.4:n.*37_*38insT
ENST00000613374.5:c.*37_*38insT	ENSP00000484464.1:n.*37_*38insT
ENST00000613706.5:c.*37_*38insT	ENSP00000484976.2:n.*37_*38insT
ENST00000617164.5:c.*37_*38insT	ENSP00000480470.1:n.*37_*38insT
ENST00000619009.5:c.*37_*38insT	ENSP00000482293.1:n.*37_*38insT
ENST00000650978.1:c.3746_3747insT
ENST00000260947.8:c.*37_*38insT	ENSP00000260947.4:n.*37_*38insT
ENST00000432456.5:c.514_515insT
ENST00000471590.5:n.706_707insT
ENST00000613374.4:c.*37_*38insT	ENSP00000484464.1:n.*37_*38insT
ENST00000613706.4:c.*37_*38insT	ENSP00000484976.1:n.*37_*38insT
ENST00000617164.4:c.*37_*38insT	ENSP00000480470.1:n.*37_*38insT
ENST00000619009.4:c.*37_*38insT	ENSP00000482293.1:n.*37_*38insT
NM_000465.3:c.*37_*38insT	NP_000456.2:n.*37_*38insT
NM_001282543.1:c.*37_*38insT	NP_001269472.1:n.*37_*38insT
NM_001282545.1:c.*37_*38insT	NP_001269474.1:n.*37_*38insT
NM_001282548.1:c.*37_*38insT	NP_001269477.1:n.*37_*38insT
NM_001282549.1:c.*37_*38insT	NP_001269478.1:n.*37_*38insT
NR_104212.1:n.2364_2365insT
NR_104215.1:n.2307_2308insT
NR_104216.1:n.1563_1564insT
XM_011511567.1:c.*37_*38insT	XP_011509869.1:n.*37_*38insT
XM_017004613.1:c.*37_*38insT	XP_016860102.1:n.*37_*38insT
XR_002959322.1:n.2737_2738insT
NM_000465.4:c.*37_*38insT MANE Select	NP_000456.2:n.*37_*38insT
NM_001282543.2:c.*37_*38insT	NP_001269472.1:n.*37_*38insT
NM_001282545.2:c.*37_*38insT	NP_001269474.1:n.*37_*38insT
NM_001282548.2:c.*37_*38insT	NP_001269477.1:n.*37_*38insT
NM_001282549.2:c.*37_*38insT	NP_001269478.1:n.*37_*38insT
NR_104212.2:n.2336_2337insT
NR_104215.2:n.2279_2280insT
NR_104216.2:n.1535_1536insT