Canonical Allele Identifier: CA431144547
Gene: BARD1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.215661790G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214797066G>A , CM000664.2:g.214797066G>A GRCh38
NC_000002.11:g.215661790G>A , CM000664.1:g.215661790G>A GRCh37
NC_000002.10:g.215370035G>A NCBI36
NG_012047.2:g.17639C>T
NG_012047.3:g.17646C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000260947.9:c.210C>T MANE Select ENSP00000260947.4:p.Phe70=
ENST00000421162.2:c.210C>T ENSP00000392245.2:p.Phe70=
ENST00000613192.2:c.158+12346C>T ENSP00000483275.2:n.158+12346C>T
ENST00000613374.5:c.158+12346C>T ENSP00000484464.1:n.158+12346C>T
ENST00000613706.5:c.210C>T ENSP00000484976.2:p.Phe70=
ENST00000617164.5:c.159-4621C>T ENSP00000480470.1:n.159-4621C>T
ENST00000619009.5:c.210C>T ENSP00000482293.1:p.Phe70=
ENST00000650978.1:c.52C>T
ENST00000260947.8:c.210C>T ENSP00000260947.4:p.Phe70=
ENST00000421162.1:c.210C>T ENSP00000392245.1:p.Phe70=
ENST00000455743.5:c.210C>T ENSP00000412186.1:p.Phe70=
ENST00000471787.1:n.259+12346C>T
ENST00000479904.1:n.301C>T
ENST00000613192.1:c.73+12346C>T ENSP00000483275.1:n.73+12346C>T
ENST00000613374.4:c.158+12346C>T ENSP00000484464.1:n.158+12346C>T
ENST00000613706.4:c.210C>T ENSP00000484976.1:p.Phe70=
ENST00000617164.4:c.159-4621C>T ENSP00000480470.1:n.159-4621C>T
ENST00000619009.4:c.210C>T ENSP00000482293.1:p.Phe70=
ENST00000620057.4:c.210C>T ENSP00000481988.1:p.Phe70=
NM_000465.3:c.210C>T NP_000456.2:p.Phe70=
NM_001282543.1:c.159-4621C>T NP_001269472.1:n.159-4621C>T
NM_001282545.1:c.210C>T NP_001269474.1:p.Phe70=
NM_001282548.1:c.158+12346C>T NP_001269477.1:n.158+12346C>T
NM_001282549.1:c.210C>T NP_001269478.1:p.Phe70=
NR_104212.1:n.352C>T
NR_104215.1:n.300+12346C>T
NR_104216.1:n.352C>T
XM_011511567.1:c.156C>T XP_011509869.1:p.Phe52=
XM_011511568.1:c.210C>T XP_011509870.1:p.Phe70=
XM_017004613.1:c.210C>T XP_016860102.1:p.Phe70=
XM_017004614.1:c.210C>T XP_016860103.1:p.Phe70=
XR_002959322.1:n.301C>T
NM_000465.4:c.210C>T MANE Select NP_000456.2:p.Phe70=
NM_001282543.2:c.159-4621C>T NP_001269472.1:n.159-4621C>T
NM_001282545.2:c.210C>T NP_001269474.1:p.Phe70=
NM_001282548.2:c.158+12346C>T NP_001269477.1:n.158+12346C>T
NM_001282549.2:c.210C>T NP_001269478.1:p.Phe70=
NR_104212.2:n.324C>T
NR_104215.2:n.272+12346C>T
NR_104216.2:n.324C>T