Canonical Allele Identifier: CA1327053361

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214745140_214745141delinsAG , CM000664.2:g.214745140_214745141delinsAG	GRCh38
NC_000002.11:g.215609864_215609865delinsAG , CM000664.1:g.215609864_215609865delinsAG	GRCh37
NC_000002.10:g.215318109_215318110delinsAG	NCBI36
NG_012047.2:g.69564_69565delinsCT
NG_012047.3:g.69571_69572delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.1829_1830delinsCT MANE Select	ENSP00000260947.4:p.Pro610=
ENST00000421162.2:c.476_477delinsCT	ENSP00000392245.2:p.Pro159=
ENST00000613192.2:c.159-14633_159-14632delinsCT	ENSP00000483275.2:n.159-14633_159-14632delinsCT
ENST00000613374.5:c.419_420delinsCT	ENSP00000484464.1:p.Pro140=
ENST00000613706.5:c.1421_1422delinsCT	ENSP00000484976.2:p.Pro474=
ENST00000617164.5:c.1772_1773delinsCT	ENSP00000480470.1:p.Pro591=
ENST00000619009.5:c.365-14633_365-14632delinsCT	ENSP00000482293.1:n.365-14633_365-14632delinsCT
ENST00000650978.1:c.3204_3205delinsCT
ENST00000260947.8:c.1829_1830delinsCT	ENSP00000260947.4:p.Pro610=
ENST00000421162.1:c.476_477delinsCT	ENSP00000392245.1:p.Pro159=
ENST00000455743.5:c.*1449_*1450delinsCT	ENSP00000412186.1:n.*1449_*1450delinsCT
ENST00000613192.1:c.74-14633_74-14632delinsCT	ENSP00000483275.1:n.74-14633_74-14632delinsCT
ENST00000613374.4:c.419_420delinsCT	ENSP00000484464.1:p.Pro140=
ENST00000613706.4:c.476_477delinsCT	ENSP00000484976.1:p.Pro159=
ENST00000617164.4:c.1772_1773delinsCT	ENSP00000480470.1:p.Pro591=
ENST00000619009.4:c.365-14633_365-14632delinsCT	ENSP00000482293.1:n.365-14633_365-14632delinsCT
ENST00000620057.4:c.*495_*496delinsCT	ENSP00000481988.1:n.*495_*496delinsCT
NM_000465.3:c.1829_1830delinsCT	NP_000456.2:p.Pro610=
NM_001282543.1:c.1772_1773delinsCT	NP_001269472.1:p.Pro591=
NM_001282545.1:c.476_477delinsCT	NP_001269474.1:p.Pro159=
NM_001282548.1:c.419_420delinsCT	NP_001269477.1:p.Pro140=
NM_001282549.1:c.365-14633_365-14632delinsCT	NP_001269478.1:n.365-14633_365-14632delinsCT
NR_104212.1:n.1822_1823delinsCT
NR_104215.1:n.1765_1766delinsCT
NR_104216.1:n.1021_1022delinsCT
XM_011511567.1:c.1775_1776delinsCT	XP_011509869.1:p.Pro592=
XM_011511568.1:c.1829_1830delinsCT	XP_011509870.1:p.Pro610=
XM_017004613.1:c.1928_1929delinsCT	XP_016860102.1:p.Pro643=
XM_017004614.1:c.1928_1929delinsCT	XP_016860103.1:p.Pro643=
XR_002959322.1:n.2019_2020delinsCT
NM_000465.4:c.1829_1830delinsCT MANE Select	NP_000456.2:p.Pro610=
NM_001282543.2:c.1772_1773delinsCT	NP_001269472.1:p.Pro591=
NM_001282545.2:c.476_477delinsCT	NP_001269474.1:p.Pro159=
NM_001282548.2:c.419_420delinsCT	NP_001269477.1:p.Pro140=
NM_001282549.2:c.365-14633_365-14632delinsCT	NP_001269478.1:n.365-14633_365-14632delinsCT
NR_104212.2:n.1794_1795delinsCT
NR_104215.2:n.1737_1738delinsCT
NR_104216.2:n.993_994delinsCT