Canonical Allele Identifier: CA16610686

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214745771C>G , CM000664.2:g.214745771C>G	GRCh38
NC_000002.11:g.215610495C>G , CM000664.1:g.215610495C>G	GRCh37
NC_000002.10:g.215318740C>G	NCBI36
NG_012047.2:g.68934G>C
NG_012047.3:g.68941G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000465.4:c.1761G>C MANE Select	NP_000456.2:p.Glu587Asp
ENST00000260947.9:c.1761G>C MANE Select	ENSP00000260947.4:p.Glu587Asp
NM_000465.3:c.1761G>C	NP_000456.2:p.Glu587Asp
NM_001282543.1:c.1704G>C	NP_001269472.1:p.Glu568Asp
NM_001282543.2:c.1704G>C	NP_001269472.1:p.Glu568Asp
NM_001282545.1:c.408G>C	NP_001269474.1:p.Glu136Asp
NM_001282545.2:c.408G>C	NP_001269474.1:p.Glu136Asp
NM_001282548.1:c.351G>C	NP_001269477.1:p.Glu117Asp
NM_001282548.2:c.351G>C	NP_001269477.1:p.Glu117Asp
NM_001282549.1:c.365-15263G>C	NP_001269478.1:n.365-15263G>C
NM_001282549.2:c.365-15263G>C	NP_001269478.1:n.365-15263G>C
NR_104212.1:n.1754G>C
NR_104212.2:n.1726G>C
NR_104215.1:n.1697G>C
NR_104215.2:n.1669G>C
NR_104216.1:n.953G>C
NR_104216.2:n.925G>C
ENST00000260947.8:c.1761G>C	ENSP00000260947.4:p.Glu587Asp
ENST00000421162.1:c.408G>C	ENSP00000392245.1:p.Glu136Asp
ENST00000421162.2:c.408G>C	ENSP00000392245.2:p.Glu136Asp
ENST00000455743.5:c.*1381G>C	ENSP00000412186.1:n.*1381G>C
ENST00000465841.1:n.116G>C
ENST00000613192.1:c.74-15263G>C	ENSP00000483275.1:n.74-15263G>C
ENST00000613192.2:c.159-15263G>C	ENSP00000483275.2:n.159-15263G>C
ENST00000613374.4:c.351G>C	ENSP00000484464.1:p.Glu117Asp
ENST00000613374.5:c.351G>C	ENSP00000484464.1:p.Glu117Asp
ENST00000613706.4:c.408G>C	ENSP00000484976.1:p.Glu136Asp
ENST00000613706.5:c.1353G>C	ENSP00000484976.2:p.Glu451Asp
ENST00000617164.4:c.1704G>C	ENSP00000480470.1:p.Glu568Asp
ENST00000617164.5:c.1704G>C	ENSP00000480470.1:p.Glu568Asp
ENST00000619009.4:c.365-15263G>C	ENSP00000482293.1:n.365-15263G>C
ENST00000619009.5:c.365-15263G>C	ENSP00000482293.1:n.365-15263G>C
ENST00000620057.4:c.*427G>C	ENSP00000481988.1:n.*427G>C
ENST00000650978.1:c.3136G>C
XM_011511567.1:c.1707G>C	XP_011509869.1:p.Glu569Asp
XM_011511568.1:c.1761G>C	XP_011509870.1:p.Glu587Asp
XM_017004613.1:c.1860G>C	XP_016860102.1:p.Glu620Asp
XM_017004614.1:c.1860G>C	XP_016860103.1:p.Glu620Asp
XR_002959322.1:n.1951G>C