Canonical Allele Identifier: CA2701493346

Gene: BARD1

Linked Data

• dbSNP Id: rs2106019285

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214745192_214745193insT , CM000664.2:g.214745192_214745193insT	GRCh38
NC_000002.11:g.215609916_215609917insT , CM000664.1:g.215609916_215609917insT	GRCh37
NC_000002.10:g.215318161_215318162insT	NCBI36
NG_012047.2:g.69512_69513insA
NG_012047.3:g.69519_69520insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.1811-34_1811-33insA MANE Select	ENSP00000260947.4:n.1811-34_1811-33insA
ENST00000421162.2:c.458-34_458-33insA	ENSP00000392245.2:n.458-34_458-33insA
ENST00000613192.2:c.159-14685_159-14684insA	ENSP00000483275.2:n.159-14685_159-14684insA
ENST00000613374.5:c.401-34_401-33insA	ENSP00000484464.1:n.401-34_401-33insA
ENST00000613706.5:c.1403-34_1403-33insA	ENSP00000484976.2:n.1403-34_1403-33insA
ENST00000617164.5:c.1754-34_1754-33insA	ENSP00000480470.1:n.1754-34_1754-33insA
ENST00000619009.5:c.365-14685_365-14684insA	ENSP00000482293.1:n.365-14685_365-14684insA
ENST00000650978.1:c.3186-34_3186-33insA
ENST00000260947.8:c.1811-34_1811-33insA	ENSP00000260947.4:n.1811-34_1811-33insA
ENST00000421162.1:c.458-34_458-33insA	ENSP00000392245.1:n.458-34_458-33insA
ENST00000455743.5:c.*1431-34_*1431-33insA	ENSP00000412186.1:n.*1431-34_*1431-33insA
ENST00000613192.1:c.74-14685_74-14684insA	ENSP00000483275.1:n.74-14685_74-14684insA
ENST00000613374.4:c.401-34_401-33insA	ENSP00000484464.1:n.401-34_401-33insA
ENST00000613706.4:c.458-34_458-33insA	ENSP00000484976.1:n.458-34_458-33insA
ENST00000617164.4:c.1754-34_1754-33insA	ENSP00000480470.1:n.1754-34_1754-33insA
ENST00000619009.4:c.365-14685_365-14684insA	ENSP00000482293.1:n.365-14685_365-14684insA
ENST00000620057.4:c.*477-34_*477-33insA	ENSP00000481988.1:n.*477-34_*477-33insA
NM_000465.3:c.1811-34_1811-33insA	NP_000456.2:n.1811-34_1811-33insA
NM_001282543.1:c.1754-34_1754-33insA	NP_001269472.1:n.1754-34_1754-33insA
NM_001282545.1:c.458-34_458-33insA	NP_001269474.1:n.458-34_458-33insA
NM_001282548.1:c.401-34_401-33insA	NP_001269477.1:n.401-34_401-33insA
NM_001282549.1:c.365-14685_365-14684insA	NP_001269478.1:n.365-14685_365-14684insA
NR_104212.1:n.1804-34_1804-33insA
NR_104215.1:n.1747-34_1747-33insA
NR_104216.1:n.1003-34_1003-33insA
XM_011511567.1:c.1757-34_1757-33insA	XP_011509869.1:n.1757-34_1757-33insA
XM_011511568.1:c.1811-34_1811-33insA	XP_011509870.1:n.1811-34_1811-33insA
XM_017004613.1:c.1910-34_1910-33insA	XP_016860102.1:n.1910-34_1910-33insA
XM_017004614.1:c.1910-34_1910-33insA	XP_016860103.1:n.1910-34_1910-33insA
XR_002959322.1:n.2001-34_2001-33insA
NM_000465.4:c.1811-34_1811-33insA MANE Select	NP_000456.2:n.1811-34_1811-33insA
NM_001282543.2:c.1754-34_1754-33insA	NP_001269472.1:n.1754-34_1754-33insA
NM_001282545.2:c.458-34_458-33insA	NP_001269474.1:n.458-34_458-33insA
NM_001282548.2:c.401-34_401-33insA	NP_001269477.1:n.401-34_401-33insA
NM_001282549.2:c.365-14685_365-14684insA	NP_001269478.1:n.365-14685_365-14684insA
NR_104212.2:n.1776-34_1776-33insA
NR_104215.2:n.1719-34_1719-33insA
NR_104216.2:n.975-34_975-33insA