Canonical Allele Identifier: CA1327053341
Gene: BARD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214745107C= , CM000664.2:g.214745107C= GRCh38
NC_000002.11:g.215609831C= , CM000664.1:g.215609831C= GRCh37
NC_000002.10:g.215318076C= NCBI36
NG_012047.2:g.69598G=
NG_012047.3:g.69605G=

Transcript Alleles

HGVS Amino-acid change
ENST00000260947.9:c.1863G= MANE Select ENSP00000260947.4:p.Met621=
ENST00000421162.2:c.510G= ENSP00000392245.2:p.Met170=
ENST00000613192.2:c.159-14599G= ENSP00000483275.2:n.159-14599G=
ENST00000613374.5:c.453G= ENSP00000484464.1:p.Met151=
ENST00000613706.5:c.1455G= ENSP00000484976.2:p.Met485=
ENST00000617164.5:c.1806G= ENSP00000480470.1:p.Met602=
ENST00000619009.5:c.365-14599G= ENSP00000482293.1:n.365-14599G=
ENST00000650978.1:c.3238G=
ENST00000260947.8:c.1863G= ENSP00000260947.4:p.Met621=
ENST00000421162.1:c.510G= ENSP00000392245.1:p.Met170=
ENST00000455743.5:c.*1483G= ENSP00000412186.1:n.*1483G=
ENST00000613192.1:c.74-14599G= ENSP00000483275.1:n.74-14599G=
ENST00000613374.4:c.453G= ENSP00000484464.1:p.Met151=
ENST00000613706.4:c.510G= ENSP00000484976.1:p.Met170=
ENST00000617164.4:c.1806G= ENSP00000480470.1:p.Met602=
ENST00000619009.4:c.365-14599G= ENSP00000482293.1:n.365-14599G=
ENST00000620057.4:c.*529G= ENSP00000481988.1:n.*529G=
NM_000465.3:c.1863G= NP_000456.2:p.Met621=
NM_001282543.1:c.1806G= NP_001269472.1:p.Met602=
NM_001282545.1:c.510G= NP_001269474.1:p.Met170=
NM_001282548.1:c.453G= NP_001269477.1:p.Met151=
NM_001282549.1:c.365-14599G= NP_001269478.1:n.365-14599G=
NR_104212.1:n.1856G=
NR_104215.1:n.1799G=
NR_104216.1:n.1055G=
XM_011511567.1:c.1809G= XP_011509869.1:p.Met603=
XM_011511568.1:c.1863G= XP_011509870.1:p.Met621=
XM_017004613.1:c.1962G= XP_016860102.1:p.Met654=
XM_017004614.1:c.1962G= XP_016860103.1:p.Met654=
XR_002959322.1:n.2053G=
NM_000465.4:c.1863G= MANE Select NP_000456.2:p.Met621=
NM_001282543.2:c.1806G= NP_001269472.1:p.Met602=
NM_001282545.2:c.510G= NP_001269474.1:p.Met170=
NM_001282548.2:c.453G= NP_001269477.1:p.Met151=
NM_001282549.2:c.365-14599G= NP_001269478.1:n.365-14599G=
NR_104212.2:n.1828G=
NR_104215.2:n.1771G=
NR_104216.2:n.1027G=