Canonical Allele Identifier: CA2701529812

Gene: BARD1

Linked Data

• dbSNP Id: rs2106107284

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214780492A>C , CM000664.2:g.214780492A>C	GRCh38
NC_000002.11:g.215645216A>C , CM000664.1:g.215645216A>C	GRCh37
NC_000002.10:g.215353461A>C	NCBI36
NG_012047.2:g.34213T>G
NG_012047.3:g.34220T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.1314+68T>G MANE Select	ENSP00000260947.4:n.1314+68T>G
ENST00000421162.2:c.215+16569T>G	ENSP00000392245.2:n.215+16569T>G
ENST00000613192.2:c.158+28920T>G	ENSP00000483275.2:n.158+28920T>G
ENST00000613374.5:c.159-27937T>G	ENSP00000484464.1:n.159-27937T>G
ENST00000613706.5:c.906+476T>G	ENSP00000484976.2:n.906+476T>G
ENST00000617164.5:c.1257+68T>G	ENSP00000480470.1:n.1257+68T>G
ENST00000619009.5:c.364+11805T>G	ENSP00000482293.1:n.364+11805T>G
ENST00000650978.1:c.1156+68T>G
ENST00000260947.8:c.1314+68T>G	ENSP00000260947.4:n.1314+68T>G
ENST00000421162.1:c.215+16569T>G	ENSP00000392245.1:n.215+16569T>G
ENST00000455743.5:c.*934+68T>G	ENSP00000412186.1:n.*934+68T>G
ENST00000613192.1:c.73+28920T>G	ENSP00000483275.1:n.73+28920T>G
ENST00000613374.4:c.159-27937T>G	ENSP00000484464.1:n.159-27937T>G
ENST00000613706.4:c.215+16569T>G	ENSP00000484976.1:n.215+16569T>G
ENST00000617164.4:c.1257+68T>G	ENSP00000480470.1:n.1257+68T>G
ENST00000619009.4:c.364+11805T>G	ENSP00000482293.1:n.364+11805T>G
ENST00000620057.4:c.365-11180T>G	ENSP00000481988.1:n.365-11180T>G
NM_000465.3:c.1314+68T>G	NP_000456.2:n.1314+68T>G
NM_001282543.1:c.1257+68T>G	NP_001269472.1:n.1257+68T>G
NM_001282545.1:c.215+16569T>G	NP_001269474.1:n.215+16569T>G
NM_001282548.1:c.159-27937T>G	NP_001269477.1:n.159-27937T>G
NM_001282549.1:c.364+11805T>G	NP_001269478.1:n.364+11805T>G
NR_104212.1:n.1307+68T>G
NR_104215.1:n.1250+68T>G
NR_104216.1:n.507-11180T>G
XM_011511567.1:c.1260+68T>G	XP_011509869.1:n.1260+68T>G
XM_011511568.1:c.1314+68T>G	XP_011509870.1:n.1314+68T>G
XM_017004613.1:c.1413+68T>G	XP_016860102.1:n.1413+68T>G
XM_017004614.1:c.1413+68T>G	XP_016860103.1:n.1413+68T>G
XR_002959322.1:n.1504+68T>G
NM_000465.4:c.1314+68T>G MANE Select	NP_000456.2:n.1314+68T>G
NM_001282543.2:c.1257+68T>G	NP_001269472.1:n.1257+68T>G
NM_001282545.2:c.215+16569T>G	NP_001269474.1:n.215+16569T>G
NM_001282548.2:c.159-27937T>G	NP_001269477.1:n.159-27937T>G
NM_001282549.2:c.364+11805T>G	NP_001269478.1:n.364+11805T>G
NR_104212.2:n.1279+68T>G
NR_104215.2:n.1222+68T>G
NR_104216.2:n.479-11180T>G