Canonical Allele Identifier: CA1327053379
Gene: BARD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214745160_214745169delinsCTAAAATACA , CM000664.2:g.214745160_214745169delinsCTAAAATACA GRCh38
NC_000002.11:g.215609884_215609893delinsCTAAAATACA , CM000664.1:g.215609884_215609893delinsCTAAAATACA GRCh37
NC_000002.10:g.215318129_215318138delinsCTAAAATACA NCBI36
NG_012047.2:g.69536_69545delinsTGTATTTTAG
NG_012047.3:g.69543_69552delinsTGTATTTTAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000260947.9:c.1811-10_1811-1delinsTGTATTTTAG MANE Select ENSP00000260947.4:n.1811-10_1811-1delinsTGTATTTTAG
ENST00000421162.2:c.458-10_458-1delinsTGTATTTTAG ENSP00000392245.2:n.458-10_458-1delinsTGTATTTTAG
ENST00000613192.2:c.159-14661_159-14652delinsTGTATTTTAG ENSP00000483275.2:n.159-14661_159-14652delinsTGTATTTTAG
ENST00000613374.5:c.401-10_401-1delinsTGTATTTTAG ENSP00000484464.1:n.401-10_401-1delinsTGTATTTTAG
ENST00000613706.5:c.1403-10_1403-1delinsTGTATTTTAG ENSP00000484976.2:n.1403-10_1403-1delinsTGTATTTTAG
ENST00000617164.5:c.1754-10_1754-1delinsTGTATTTTAG ENSP00000480470.1:n.1754-10_1754-1delinsTGTATTTTAG
ENST00000619009.5:c.365-14661_365-14652delinsTGTATTTTAG ENSP00000482293.1:n.365-14661_365-14652delinsTGTATTTTAG
ENST00000650978.1:c.3186-10_3186-1delinsTGTATTTTAG
ENST00000260947.8:c.1811-10_1811-1delinsTGTATTTTAG ENSP00000260947.4:n.1811-10_1811-1delinsTGTATTTTAG
ENST00000421162.1:c.458-10_458-1delinsTGTATTTTAG ENSP00000392245.1:n.458-10_458-1delinsTGTATTTTAG
ENST00000455743.5:c.*1431-10_*1431-1delinsTGTATTTTAG ENSP00000412186.1:n.*1431-10_*1431-1delinsTGTATTTTAG
ENST00000613192.1:c.74-14661_74-14652delinsTGTATTTTAG ENSP00000483275.1:n.74-14661_74-14652delinsTGTATTTTAG
ENST00000613374.4:c.401-10_401-1delinsTGTATTTTAG ENSP00000484464.1:n.401-10_401-1delinsTGTATTTTAG
ENST00000613706.4:c.458-10_458-1delinsTGTATTTTAG ENSP00000484976.1:n.458-10_458-1delinsTGTATTTTAG
ENST00000617164.4:c.1754-10_1754-1delinsTGTATTTTAG ENSP00000480470.1:n.1754-10_1754-1delinsTGTATTTTAG
ENST00000619009.4:c.365-14661_365-14652delinsTGTATTTTAG ENSP00000482293.1:n.365-14661_365-14652delinsTGTATTTTAG
ENST00000620057.4:c.*477-10_*477-1delinsTGTATTTTAG ENSP00000481988.1:n.*477-10_*477-1delinsTGTATTTTAG
NM_000465.3:c.1811-10_1811-1delinsTGTATTTTAG NP_000456.2:n.1811-10_1811-1delinsTGTATTTTAG
NM_001282543.1:c.1754-10_1754-1delinsTGTATTTTAG NP_001269472.1:n.1754-10_1754-1delinsTGTATTTTAG
NM_001282545.1:c.458-10_458-1delinsTGTATTTTAG NP_001269474.1:n.458-10_458-1delinsTGTATTTTAG
NM_001282548.1:c.401-10_401-1delinsTGTATTTTAG NP_001269477.1:n.401-10_401-1delinsTGTATTTTAG
NM_001282549.1:c.365-14661_365-14652delinsTGTATTTTAG NP_001269478.1:n.365-14661_365-14652delinsTGTATTTTAG
NR_104212.1:n.1804-10_1804-1delinsTGTATTTTAG
NR_104215.1:n.1747-10_1747-1delinsTGTATTTTAG
NR_104216.1:n.1003-10_1003-1delinsTGTATTTTAG
XM_011511567.1:c.1757-10_1757-1delinsTGTATTTTAG XP_011509869.1:n.1757-10_1757-1delinsTGTATTTTAG
XM_011511568.1:c.1811-10_1811-1delinsTGTATTTTAG XP_011509870.1:n.1811-10_1811-1delinsTGTATTTTAG
XM_017004613.1:c.1910-10_1910-1delinsTGTATTTTAG XP_016860102.1:n.1910-10_1910-1delinsTGTATTTTAG
XM_017004614.1:c.1910-10_1910-1delinsTGTATTTTAG XP_016860103.1:n.1910-10_1910-1delinsTGTATTTTAG
XR_002959322.1:n.2001-10_2001-1delinsTGTATTTTAG
NM_000465.4:c.1811-10_1811-1delinsTGTATTTTAG MANE Select NP_000456.2:n.1811-10_1811-1delinsTGTATTTTAG
NM_001282543.2:c.1754-10_1754-1delinsTGTATTTTAG NP_001269472.1:n.1754-10_1754-1delinsTGTATTTTAG
NM_001282545.2:c.458-10_458-1delinsTGTATTTTAG NP_001269474.1:n.458-10_458-1delinsTGTATTTTAG
NM_001282548.2:c.401-10_401-1delinsTGTATTTTAG NP_001269477.1:n.401-10_401-1delinsTGTATTTTAG
NM_001282549.2:c.365-14661_365-14652delinsTGTATTTTAG NP_001269478.1:n.365-14661_365-14652delinsTGTATTTTAG
NR_104212.2:n.1776-10_1776-1delinsTGTATTTTAG
NR_104215.2:n.1719-10_1719-1delinsTGTATTTTAG
NR_104216.2:n.975-10_975-1delinsTGTATTTTAG