Canonical Allele Identifier: CA350454413

Gene: BARD1

Linked Data

• ClinVar Variation Id: 2713875
• ClinVar RCV Id: RCV003501355
• MyVariant Identifiers: chr2:g.215645594C>A (hg19) ; chr2:g.214780870C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214780870C>A , CM000664.2:g.214780870C>A	GRCh38
NC_000002.11:g.215645594C>A , CM000664.1:g.215645594C>A	GRCh37
NC_000002.10:g.215353839C>A	NCBI36
NG_012047.2:g.33835G>T
NG_012047.3:g.33842G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.1004G>T MANE Select	ENSP00000260947.4:p.Arg335Ile
ENST00000421162.2:c.215+16191G>T	ENSP00000392245.2:n.215+16191G>T
ENST00000613192.2:c.158+28542G>T	ENSP00000483275.2:n.158+28542G>T
ENST00000613374.5:c.159-28315G>T	ENSP00000484464.1:n.159-28315G>T
ENST00000613706.5:c.906+98G>T	ENSP00000484976.2:n.906+98G>T
ENST00000617164.5:c.947G>T	ENSP00000480470.1:p.Arg316Ile
ENST00000619009.5:c.364+11427G>T	ENSP00000482293.1:n.364+11427G>T
ENST00000650978.1:c.846G>T
ENST00000260947.8:c.1004G>T	ENSP00000260947.4:p.Arg335Ile
ENST00000421162.1:c.215+16191G>T	ENSP00000392245.1:n.215+16191G>T
ENST00000455743.5:c.*624G>T	ENSP00000412186.1:n.*624G>T
ENST00000613192.1:c.73+28542G>T	ENSP00000483275.1:n.73+28542G>T
ENST00000613374.4:c.159-28315G>T	ENSP00000484464.1:n.159-28315G>T
ENST00000613706.4:c.215+16191G>T	ENSP00000484976.1:n.215+16191G>T
ENST00000617164.4:c.947G>T	ENSP00000480470.1:p.Arg316Ile
ENST00000619009.4:c.364+11427G>T	ENSP00000482293.1:n.364+11427G>T
ENST00000620057.4:c.364+11427G>T	ENSP00000481988.1:n.364+11427G>T
NM_000465.3:c.1004G>T	NP_000456.2:p.Arg335Ile
NM_001282543.1:c.947G>T	NP_001269472.1:p.Arg316Ile
NM_001282545.1:c.215+16191G>T	NP_001269474.1:n.215+16191G>T
NM_001282548.1:c.159-28315G>T	NP_001269477.1:n.159-28315G>T
NM_001282549.1:c.364+11427G>T	NP_001269478.1:n.364+11427G>T
NR_104212.1:n.997G>T
NR_104215.1:n.940G>T
NR_104216.1:n.506+11427G>T
XM_011511567.1:c.950G>T	XP_011509869.1:p.Arg317Ile
XM_011511568.1:c.1004G>T	XP_011509870.1:p.Arg335Ile
XM_017004613.1:c.1103G>T	XP_016860102.1:p.Arg368Ile
XM_017004614.1:c.1103G>T	XP_016860103.1:p.Arg368Ile
XR_002959322.1:n.1194G>T
NM_000465.4:c.1004G>T MANE Select	NP_000456.2:p.Arg335Ile
NM_001282543.2:c.947G>T	NP_001269472.1:p.Arg316Ile
NM_001282545.2:c.215+16191G>T	NP_001269474.1:n.215+16191G>T
NM_001282548.2:c.159-28315G>T	NP_001269477.1:n.159-28315G>T
NM_001282549.2:c.364+11427G>T	NP_001269478.1:n.364+11427G>T
NR_104212.2:n.969G>T
NR_104215.2:n.912G>T
NR_104216.2:n.478+11427G>T