Canonical Allele Identifier: CA431145449
Gene: BARD1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.215609882T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214745158T>C , CM000664.2:g.214745158T>C GRCh38
NC_000002.11:g.215609882T>C , CM000664.1:g.215609882T>C GRCh37
NC_000002.10:g.215318127T>C NCBI36
NG_012047.2:g.69547A>G
NG_012047.3:g.69554A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000260947.9:c.1812A>G MANE Select ENSP00000260947.4:p.Val604=
ENST00000421162.2:c.459A>G ENSP00000392245.2:p.Val153=
ENST00000613192.2:c.159-14650A>G ENSP00000483275.2:n.159-14650A>G
ENST00000613374.5:c.402A>G ENSP00000484464.1:p.Val134=
ENST00000613706.5:c.1404A>G ENSP00000484976.2:p.Val468=
ENST00000617164.5:c.1755A>G ENSP00000480470.1:p.Val585=
ENST00000619009.5:c.365-14650A>G ENSP00000482293.1:n.365-14650A>G
ENST00000650978.1:c.3187A>G
ENST00000260947.8:c.1812A>G ENSP00000260947.4:p.Val604=
ENST00000421162.1:c.459A>G ENSP00000392245.1:p.Val153=
ENST00000455743.5:c.*1432A>G ENSP00000412186.1:n.*1432A>G
ENST00000613192.1:c.74-14650A>G ENSP00000483275.1:n.74-14650A>G
ENST00000613374.4:c.402A>G ENSP00000484464.1:p.Val134=
ENST00000613706.4:c.459A>G ENSP00000484976.1:p.Val153=
ENST00000617164.4:c.1755A>G ENSP00000480470.1:p.Val585=
ENST00000619009.4:c.365-14650A>G ENSP00000482293.1:n.365-14650A>G
ENST00000620057.4:c.*478A>G ENSP00000481988.1:n.*478A>G
NM_000465.3:c.1812A>G NP_000456.2:p.Val604=
NM_001282543.1:c.1755A>G NP_001269472.1:p.Val585=
NM_001282545.1:c.459A>G NP_001269474.1:p.Val153=
NM_001282548.1:c.402A>G NP_001269477.1:p.Val134=
NM_001282549.1:c.365-14650A>G NP_001269478.1:n.365-14650A>G
NR_104212.1:n.1805A>G
NR_104215.1:n.1748A>G
NR_104216.1:n.1004A>G
XM_011511567.1:c.1758A>G XP_011509869.1:p.Val586=
XM_011511568.1:c.1812A>G XP_011509870.1:p.Val604=
XM_017004613.1:c.1911A>G XP_016860102.1:p.Val637=
XM_017004614.1:c.1911A>G XP_016860103.1:p.Val637=
XR_002959322.1:n.2002A>G
NM_000465.4:c.1812A>G MANE Select NP_000456.2:p.Val604=
NM_001282543.2:c.1755A>G NP_001269472.1:p.Val585=
NM_001282545.2:c.459A>G NP_001269474.1:p.Val153=
NM_001282548.2:c.402A>G NP_001269477.1:p.Val134=
NM_001282549.2:c.365-14650A>G NP_001269478.1:n.365-14650A>G
NR_104212.2:n.1777A>G
NR_104215.2:n.1720A>G
NR_104216.2:n.976A>G