Canonical Allele Identifier: CA350451231
Gene: BARD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214730477A>C , CM000664.2:g.214730477A>C GRCh38
NC_000002.11:g.215595201A>C , CM000664.1:g.215595201A>C GRCh37
NC_000002.10:g.215303446A>C NCBI36
NG_012047.2:g.84228T>G
NG_012047.3:g.84235T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000260947.9:c.1935T>G MANE Select ENSP00000260947.4:p.Cys645Trp
ENST00000421162.2:c.582T>G ENSP00000392245.2:p.Cys194Trp
ENST00000613192.2:c.190T>G ENSP00000483275.2:p.Ter64Gly
ENST00000613374.5:c.525T>G ENSP00000484464.1:p.Cys175Trp
ENST00000613706.5:c.1527T>G ENSP00000484976.2:p.Cys509Trp
ENST00000617164.5:c.1878T>G ENSP00000480470.1:p.Cys626Trp
ENST00000619009.5:c.396T>G ENSP00000482293.1:p.Cys132Trp
ENST00000650978.1:c.3310T>G
ENST00000260947.8:c.1935T>G ENSP00000260947.4:p.Cys645Trp
ENST00000421162.1:c.582T>G ENSP00000392245.1:p.Cys194Trp
ENST00000432456.5:c.32T>G
ENST00000455743.5:c.*1555T>G ENSP00000412186.1:n.*1555T>G
ENST00000471590.5:n.270T>G
ENST00000613192.1:c.105T>G ENSP00000483275.1:p.Cys35Trp
ENST00000613374.4:c.525T>G ENSP00000484464.1:p.Cys175Trp
ENST00000613706.4:c.582T>G ENSP00000484976.1:p.Cys194Trp
ENST00000617164.4:c.1878T>G ENSP00000480470.1:p.Cys626Trp
ENST00000619009.4:c.396T>G ENSP00000482293.1:p.Cys132Trp
ENST00000620057.4:c.*601T>G ENSP00000481988.1:n.*601T>G
NM_000465.3:c.1935T>G NP_000456.2:p.Cys645Trp
NM_001282543.1:c.1878T>G NP_001269472.1:p.Cys626Trp
NM_001282545.1:c.582T>G NP_001269474.1:p.Cys194Trp
NM_001282548.1:c.525T>G NP_001269477.1:p.Cys175Trp
NM_001282549.1:c.396T>G NP_001269478.1:p.Cys132Trp
NR_104212.1:n.1928T>G
NR_104215.1:n.1871T>G
NR_104216.1:n.1127T>G
XM_011511567.1:c.1881T>G XP_011509869.1:p.Cys627Trp
XM_017004613.1:c.2034T>G XP_016860102.1:p.Cys678Trp
XR_002959322.1:n.2125T>G
NM_000465.4:c.1935T>G MANE Select NP_000456.2:p.Cys645Trp
NM_001282543.2:c.1878T>G NP_001269472.1:p.Cys626Trp
NM_001282545.2:c.582T>G NP_001269474.1:p.Cys194Trp
NM_001282548.2:c.525T>G NP_001269477.1:p.Cys175Trp
NM_001282549.2:c.396T>G NP_001269478.1:p.Cys132Trp
NR_104212.2:n.1900T>G
NR_104215.2:n.1843T>G
NR_104216.2:n.1099T>G