Canonical Allele Identifier: CA1327053392

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214745183_214745187delinsGAGAA , CM000664.2:g.214745183_214745187delinsGAGAA	GRCh38
NC_000002.11:g.215609907_215609911delinsGAGAA , CM000664.1:g.215609907_215609911delinsGAGAA	GRCh37
NC_000002.10:g.215318152_215318156delinsGAGAA	NCBI36
NG_012047.2:g.69518_69522delinsTTCTC
NG_012047.3:g.69525_69529delinsTTCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.1811-28_1811-24delinsTTCTC MANE Select	ENSP00000260947.4:n.1811-28_1811-24delinsTTCTC
ENST00000421162.2:c.458-28_458-24delinsTTCTC	ENSP00000392245.2:n.458-28_458-24delinsTTCTC
ENST00000613192.2:c.159-14679_159-14675delinsTTCTC	ENSP00000483275.2:n.159-14679_159-14675delinsTTCTC
ENST00000613374.5:c.401-28_401-24delinsTTCTC	ENSP00000484464.1:n.401-28_401-24delinsTTCTC
ENST00000613706.5:c.1403-28_1403-24delinsTTCTC	ENSP00000484976.2:n.1403-28_1403-24delinsTTCTC
ENST00000617164.5:c.1754-28_1754-24delinsTTCTC	ENSP00000480470.1:n.1754-28_1754-24delinsTTCTC
ENST00000619009.5:c.365-14679_365-14675delinsTTCTC	ENSP00000482293.1:n.365-14679_365-14675delinsTTCTC
ENST00000650978.1:c.3186-28_3186-24delinsTTCTC
ENST00000260947.8:c.1811-28_1811-24delinsTTCTC	ENSP00000260947.4:n.1811-28_1811-24delinsTTCTC
ENST00000421162.1:c.458-28_458-24delinsTTCTC	ENSP00000392245.1:n.458-28_458-24delinsTTCTC
ENST00000455743.5:c.*1431-28_*1431-24delinsTTCTC	ENSP00000412186.1:n.*1431-28_*1431-24delinsTTCTC
ENST00000613192.1:c.74-14679_74-14675delinsTTCTC	ENSP00000483275.1:n.74-14679_74-14675delinsTTCTC
ENST00000613374.4:c.401-28_401-24delinsTTCTC	ENSP00000484464.1:n.401-28_401-24delinsTTCTC
ENST00000613706.4:c.458-28_458-24delinsTTCTC	ENSP00000484976.1:n.458-28_458-24delinsTTCTC
ENST00000617164.4:c.1754-28_1754-24delinsTTCTC	ENSP00000480470.1:n.1754-28_1754-24delinsTTCTC
ENST00000619009.4:c.365-14679_365-14675delinsTTCTC	ENSP00000482293.1:n.365-14679_365-14675delinsTTCTC
ENST00000620057.4:c.*477-28_*477-24delinsTTCTC	ENSP00000481988.1:n.*477-28_*477-24delinsTTCTC
NM_000465.3:c.1811-28_1811-24delinsTTCTC	NP_000456.2:n.1811-28_1811-24delinsTTCTC
NM_001282543.1:c.1754-28_1754-24delinsTTCTC	NP_001269472.1:n.1754-28_1754-24delinsTTCTC
NM_001282545.1:c.458-28_458-24delinsTTCTC	NP_001269474.1:n.458-28_458-24delinsTTCTC
NM_001282548.1:c.401-28_401-24delinsTTCTC	NP_001269477.1:n.401-28_401-24delinsTTCTC
NM_001282549.1:c.365-14679_365-14675delinsTTCTC	NP_001269478.1:n.365-14679_365-14675delinsTTCTC
NR_104212.1:n.1804-28_1804-24delinsTTCTC
NR_104215.1:n.1747-28_1747-24delinsTTCTC
NR_104216.1:n.1003-28_1003-24delinsTTCTC
XM_011511567.1:c.1757-28_1757-24delinsTTCTC	XP_011509869.1:n.1757-28_1757-24delinsTTCTC
XM_011511568.1:c.1811-28_1811-24delinsTTCTC	XP_011509870.1:n.1811-28_1811-24delinsTTCTC
XM_017004613.1:c.1910-28_1910-24delinsTTCTC	XP_016860102.1:n.1910-28_1910-24delinsTTCTC
XM_017004614.1:c.1910-28_1910-24delinsTTCTC	XP_016860103.1:n.1910-28_1910-24delinsTTCTC
XR_002959322.1:n.2001-28_2001-24delinsTTCTC
NM_000465.4:c.1811-28_1811-24delinsTTCTC MANE Select	NP_000456.2:n.1811-28_1811-24delinsTTCTC
NM_001282543.2:c.1754-28_1754-24delinsTTCTC	NP_001269472.1:n.1754-28_1754-24delinsTTCTC
NM_001282545.2:c.458-28_458-24delinsTTCTC	NP_001269474.1:n.458-28_458-24delinsTTCTC
NM_001282548.2:c.401-28_401-24delinsTTCTC	NP_001269477.1:n.401-28_401-24delinsTTCTC
NM_001282549.2:c.365-14679_365-14675delinsTTCTC	NP_001269478.1:n.365-14679_365-14675delinsTTCTC
NR_104212.2:n.1776-28_1776-24delinsTTCTC
NR_104215.2:n.1719-28_1719-24delinsTTCTC
NR_104216.2:n.975-28_975-24delinsTTCTC