Canonical Allele Identifier: CA350452097

Gene: BARD1

Linked Data

• MyVariant Identifiers: chr2:g.215609815C>G (hg19) ; chr2:g.214745091C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214745091C>G , CM000664.2:g.214745091C>G	GRCh38
NC_000002.11:g.215609815C>G , CM000664.1:g.215609815C>G	GRCh37
NC_000002.10:g.215318060C>G	NCBI36
NG_012047.2:g.69614G>C
NG_012047.3:g.69621G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.1879G>C MANE Select	ENSP00000260947.4:p.Gly627Arg
ENST00000421162.2:c.526G>C	ENSP00000392245.2:p.Gly176Arg
ENST00000613192.2:c.159-14583G>C	ENSP00000483275.2:n.159-14583G>C
ENST00000613374.5:c.469G>C	ENSP00000484464.1:p.Gly157Arg
ENST00000613706.5:c.1471G>C	ENSP00000484976.2:p.Gly491Arg
ENST00000617164.5:c.1822G>C	ENSP00000480470.1:p.Gly608Arg
ENST00000619009.5:c.365-14583G>C	ENSP00000482293.1:n.365-14583G>C
ENST00000650978.1:c.3254G>C
ENST00000260947.8:c.1879G>C	ENSP00000260947.4:p.Gly627Arg
ENST00000421162.1:c.526G>C	ENSP00000392245.1:p.Gly176Arg
ENST00000455743.5:c.*1499G>C	ENSP00000412186.1:n.*1499G>C
ENST00000613192.1:c.74-14583G>C	ENSP00000483275.1:n.74-14583G>C
ENST00000613374.4:c.469G>C	ENSP00000484464.1:p.Gly157Arg
ENST00000613706.4:c.526G>C	ENSP00000484976.1:p.Gly176Arg
ENST00000617164.4:c.1822G>C	ENSP00000480470.1:p.Gly608Arg
ENST00000619009.4:c.365-14583G>C	ENSP00000482293.1:n.365-14583G>C
ENST00000620057.4:c.*545G>C	ENSP00000481988.1:n.*545G>C
NM_000465.3:c.1879G>C	NP_000456.2:p.Gly627Arg
NM_001282543.1:c.1822G>C	NP_001269472.1:p.Gly608Arg
NM_001282545.1:c.526G>C	NP_001269474.1:p.Gly176Arg
NM_001282548.1:c.469G>C	NP_001269477.1:p.Gly157Arg
NM_001282549.1:c.365-14583G>C	NP_001269478.1:n.365-14583G>C
NR_104212.1:n.1872G>C
NR_104215.1:n.1815G>C
NR_104216.1:n.1071G>C
XM_011511567.1:c.1825G>C	XP_011509869.1:p.Gly609Arg
XM_011511568.1:c.1879G>C	XP_011509870.1:p.Gly627Arg
XM_017004613.1:c.1978G>C	XP_016860102.1:p.Gly660Arg
XM_017004614.1:c.1978G>C	XP_016860103.1:p.Gly660Arg
XR_002959322.1:n.2069G>C
NM_000465.4:c.1879G>C MANE Select	NP_000456.2:p.Gly627Arg
NM_001282543.2:c.1822G>C	NP_001269472.1:p.Gly608Arg
NM_001282545.2:c.526G>C	NP_001269474.1:p.Gly176Arg
NM_001282548.2:c.469G>C	NP_001269477.1:p.Gly157Arg
NM_001282549.2:c.365-14583G>C	NP_001269478.1:n.365-14583G>C
NR_104212.2:n.1844G>C
NR_104215.2:n.1787G>C
NR_104216.2:n.1043G>C