Canonical Allele Identifier: CA350458223

Gene: BARD1

Linked Data

• MyVariant Identifiers: chr2:g.215646212C>G (hg19) ; chr2:g.214781488C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214781488C>G , CM000664.2:g.214781488C>G	GRCh38
NC_000002.11:g.215646212C>G , CM000664.1:g.215646212C>G	GRCh37
NC_000002.10:g.215354457C>G	NCBI36
NG_012047.2:g.33217G>C
NG_012047.3:g.33224G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.386G>C MANE Select	ENSP00000260947.4:p.Arg129Thr
ENST00000421162.2:c.215+15573G>C	ENSP00000392245.2:n.215+15573G>C
ENST00000613192.2:c.158+27924G>C	ENSP00000483275.2:n.158+27924G>C
ENST00000613374.5:c.158+27924G>C	ENSP00000484464.1:n.158+27924G>C
ENST00000613706.5:c.386G>C	ENSP00000484976.2:p.Arg129Thr
ENST00000617164.5:c.329G>C	ENSP00000480470.1:p.Arg110Thr
ENST00000619009.5:c.364+10809G>C	ENSP00000482293.1:n.364+10809G>C
ENST00000650978.1:c.228G>C
ENST00000260947.8:c.386G>C	ENSP00000260947.4:p.Arg129Thr
ENST00000421162.1:c.215+15573G>C	ENSP00000392245.1:n.215+15573G>C
ENST00000455743.5:c.*6G>C	ENSP00000412186.1:n.*6G>C
ENST00000471787.1:n.281G>C
ENST00000613192.1:c.73+27924G>C	ENSP00000483275.1:n.73+27924G>C
ENST00000613374.4:c.158+27924G>C	ENSP00000484464.1:n.158+27924G>C
ENST00000613706.4:c.215+15573G>C	ENSP00000484976.1:n.215+15573G>C
ENST00000617164.4:c.329G>C	ENSP00000480470.1:p.Arg110Thr
ENST00000619009.4:c.364+10809G>C	ENSP00000482293.1:n.364+10809G>C
ENST00000620057.4:c.364+10809G>C	ENSP00000481988.1:n.364+10809G>C
NM_000465.3:c.386G>C	NP_000456.2:p.Arg129Thr
NM_001282543.1:c.329G>C	NP_001269472.1:p.Arg110Thr
NM_001282545.1:c.215+15573G>C	NP_001269474.1:n.215+15573G>C
NM_001282548.1:c.158+27924G>C	NP_001269477.1:n.158+27924G>C
NM_001282549.1:c.364+10809G>C	NP_001269478.1:n.364+10809G>C
NR_104212.1:n.379G>C
NR_104215.1:n.322G>C
NR_104216.1:n.506+10809G>C
XM_011511567.1:c.332G>C	XP_011509869.1:p.Arg111Thr
XM_011511568.1:c.386G>C	XP_011509870.1:p.Arg129Thr
XM_017004613.1:c.485G>C	XP_016860102.1:p.Arg162Thr
XM_017004614.1:c.485G>C	XP_016860103.1:p.Arg162Thr
XR_002959322.1:n.576G>C
NM_000465.4:c.386G>C MANE Select	NP_000456.2:p.Arg129Thr
NM_001282543.2:c.329G>C	NP_001269472.1:p.Arg110Thr
NM_001282545.2:c.215+15573G>C	NP_001269474.1:n.215+15573G>C
NM_001282548.2:c.158+27924G>C	NP_001269477.1:n.158+27924G>C
NM_001282549.2:c.364+10809G>C	NP_001269478.1:n.364+10809G>C
NR_104212.2:n.351G>C
NR_104215.2:n.294G>C
NR_104216.2:n.478+10809G>C