Canonical Allele Identifier: CA2662969901

Gene: BARD1

Linked Data

• gnomAD v4: 2-214745160-C-CTG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214745161_214745162insGT , CM000664.2:g.214745161_214745162insGT	GRCh38
NC_000002.11:g.215609885_215609886insGT , CM000664.1:g.215609885_215609886insGT	GRCh37
NC_000002.10:g.215318130_215318131insGT	NCBI36
NG_012047.2:g.69544_69545insCA
NG_012047.3:g.69551_69552insCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.1811-2_1811-1insCA MANE Select	ENSP00000260947.4:n.1811-2_1811-1insCA
ENST00000421162.2:c.458-2_458-1insCA	ENSP00000392245.2:n.458-2_458-1insCA
ENST00000613192.2:c.159-14653_159-14652insCA	ENSP00000483275.2:n.159-14653_159-14652insCA
ENST00000613374.5:c.401-2_401-1insCA	ENSP00000484464.1:n.401-2_401-1insCA
ENST00000613706.5:c.1403-2_1403-1insCA	ENSP00000484976.2:n.1403-2_1403-1insCA
ENST00000617164.5:c.1754-2_1754-1insCA	ENSP00000480470.1:n.1754-2_1754-1insCA
ENST00000619009.5:c.365-14653_365-14652insCA	ENSP00000482293.1:n.365-14653_365-14652insCA
ENST00000650978.1:c.3186-2_3186-1insCA
ENST00000260947.8:c.1811-2_1811-1insCA	ENSP00000260947.4:n.1811-2_1811-1insCA
ENST00000421162.1:c.458-2_458-1insCA	ENSP00000392245.1:n.458-2_458-1insCA
ENST00000455743.5:c.*1431-2_*1431-1insCA	ENSP00000412186.1:n.*1431-2_*1431-1insCA
ENST00000613192.1:c.74-14653_74-14652insCA	ENSP00000483275.1:n.74-14653_74-14652insCA
ENST00000613374.4:c.401-2_401-1insCA	ENSP00000484464.1:n.401-2_401-1insCA
ENST00000613706.4:c.458-2_458-1insCA	ENSP00000484976.1:n.458-2_458-1insCA
ENST00000617164.4:c.1754-2_1754-1insCA	ENSP00000480470.1:n.1754-2_1754-1insCA
ENST00000619009.4:c.365-14653_365-14652insCA	ENSP00000482293.1:n.365-14653_365-14652insCA
ENST00000620057.4:c.*477-2_*477-1insCA	ENSP00000481988.1:n.*477-2_*477-1insCA
NM_000465.3:c.1811-2_1811-1insCA	NP_000456.2:n.1811-2_1811-1insCA
NM_001282543.1:c.1754-2_1754-1insCA	NP_001269472.1:n.1754-2_1754-1insCA
NM_001282545.1:c.458-2_458-1insCA	NP_001269474.1:n.458-2_458-1insCA
NM_001282548.1:c.401-2_401-1insCA	NP_001269477.1:n.401-2_401-1insCA
NM_001282549.1:c.365-14653_365-14652insCA	NP_001269478.1:n.365-14653_365-14652insCA
NR_104212.1:n.1804-2_1804-1insCA
NR_104215.1:n.1747-2_1747-1insCA
NR_104216.1:n.1003-2_1003-1insCA
XM_011511567.1:c.1757-2_1757-1insCA	XP_011509869.1:n.1757-2_1757-1insCA
XM_011511568.1:c.1811-2_1811-1insCA	XP_011509870.1:n.1811-2_1811-1insCA
XM_017004613.1:c.1910-2_1910-1insCA	XP_016860102.1:n.1910-2_1910-1insCA
XM_017004614.1:c.1910-2_1910-1insCA	XP_016860103.1:n.1910-2_1910-1insCA
XR_002959322.1:n.2001-2_2001-1insCA
NM_000465.4:c.1811-2_1811-1insCA MANE Select	NP_000456.2:n.1811-2_1811-1insCA
NM_001282543.2:c.1754-2_1754-1insCA	NP_001269472.1:n.1754-2_1754-1insCA
NM_001282545.2:c.458-2_458-1insCA	NP_001269474.1:n.458-2_458-1insCA
NM_001282548.2:c.401-2_401-1insCA	NP_001269477.1:n.401-2_401-1insCA
NM_001282549.2:c.365-14653_365-14652insCA	NP_001269478.1:n.365-14653_365-14652insCA
NR_104212.2:n.1776-2_1776-1insCA
NR_104215.2:n.1719-2_1719-1insCA
NR_104216.2:n.975-2_975-1insCA