Canonical Allele Identifier: CA1327053394

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214745189_214745190delinsGA , CM000664.2:g.214745189_214745190delinsGA	GRCh38
NC_000002.11:g.215609913_215609914delinsGA , CM000664.1:g.215609913_215609914delinsGA	GRCh37
NC_000002.10:g.215318158_215318159delinsGA	NCBI36
NG_012047.2:g.69515_69516delinsTC
NG_012047.3:g.69522_69523delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.1811-31_1811-30delinsTC MANE Select	ENSP00000260947.4:n.1811-31_1811-30delinsTC
ENST00000421162.2:c.458-31_458-30delinsTC	ENSP00000392245.2:n.458-31_458-30delinsTC
ENST00000613192.2:c.159-14682_159-14681delinsTC	ENSP00000483275.2:n.159-14682_159-14681delinsTC
ENST00000613374.5:c.401-31_401-30delinsTC	ENSP00000484464.1:n.401-31_401-30delinsTC
ENST00000613706.5:c.1403-31_1403-30delinsTC	ENSP00000484976.2:n.1403-31_1403-30delinsTC
ENST00000617164.5:c.1754-31_1754-30delinsTC	ENSP00000480470.1:n.1754-31_1754-30delinsTC
ENST00000619009.5:c.365-14682_365-14681delinsTC	ENSP00000482293.1:n.365-14682_365-14681delinsTC
ENST00000650978.1:c.3186-31_3186-30delinsTC
ENST00000260947.8:c.1811-31_1811-30delinsTC	ENSP00000260947.4:n.1811-31_1811-30delinsTC
ENST00000421162.1:c.458-31_458-30delinsTC	ENSP00000392245.1:n.458-31_458-30delinsTC
ENST00000455743.5:c.*1431-31_*1431-30delinsTC	ENSP00000412186.1:n.*1431-31_*1431-30delinsTC
ENST00000613192.1:c.74-14682_74-14681delinsTC	ENSP00000483275.1:n.74-14682_74-14681delinsTC
ENST00000613374.4:c.401-31_401-30delinsTC	ENSP00000484464.1:n.401-31_401-30delinsTC
ENST00000613706.4:c.458-31_458-30delinsTC	ENSP00000484976.1:n.458-31_458-30delinsTC
ENST00000617164.4:c.1754-31_1754-30delinsTC	ENSP00000480470.1:n.1754-31_1754-30delinsTC
ENST00000619009.4:c.365-14682_365-14681delinsTC	ENSP00000482293.1:n.365-14682_365-14681delinsTC
ENST00000620057.4:c.*477-31_*477-30delinsTC	ENSP00000481988.1:n.*477-31_*477-30delinsTC
NM_000465.3:c.1811-31_1811-30delinsTC	NP_000456.2:n.1811-31_1811-30delinsTC
NM_001282543.1:c.1754-31_1754-30delinsTC	NP_001269472.1:n.1754-31_1754-30delinsTC
NM_001282545.1:c.458-31_458-30delinsTC	NP_001269474.1:n.458-31_458-30delinsTC
NM_001282548.1:c.401-31_401-30delinsTC	NP_001269477.1:n.401-31_401-30delinsTC
NM_001282549.1:c.365-14682_365-14681delinsTC	NP_001269478.1:n.365-14682_365-14681delinsTC
NR_104212.1:n.1804-31_1804-30delinsTC
NR_104215.1:n.1747-31_1747-30delinsTC
NR_104216.1:n.1003-31_1003-30delinsTC
XM_011511567.1:c.1757-31_1757-30delinsTC	XP_011509869.1:n.1757-31_1757-30delinsTC
XM_011511568.1:c.1811-31_1811-30delinsTC	XP_011509870.1:n.1811-31_1811-30delinsTC
XM_017004613.1:c.1910-31_1910-30delinsTC	XP_016860102.1:n.1910-31_1910-30delinsTC
XM_017004614.1:c.1910-31_1910-30delinsTC	XP_016860103.1:n.1910-31_1910-30delinsTC
XR_002959322.1:n.2001-31_2001-30delinsTC
NM_000465.4:c.1811-31_1811-30delinsTC MANE Select	NP_000456.2:n.1811-31_1811-30delinsTC
NM_001282543.2:c.1754-31_1754-30delinsTC	NP_001269472.1:n.1754-31_1754-30delinsTC
NM_001282545.2:c.458-31_458-30delinsTC	NP_001269474.1:n.458-31_458-30delinsTC
NM_001282548.2:c.401-31_401-30delinsTC	NP_001269477.1:n.401-31_401-30delinsTC
NM_001282549.2:c.365-14682_365-14681delinsTC	NP_001269478.1:n.365-14682_365-14681delinsTC
NR_104212.2:n.1776-31_1776-30delinsTC
NR_104215.2:n.1719-31_1719-30delinsTC
NR_104216.2:n.975-31_975-30delinsTC