Canonical Allele Identifier: CA350453628

Gene: BARD1

Linked Data

• ClinVar Variation Id: 1057255
• ClinVar RCV Id: RCV001366201 ; RCV001776227 ; RCV002368184
• dbSNP Id: rs786203825
• gnomAD v4: 2-214780643-G-A
• COSMIC: COSM5607934 ; COSM5607935
• MyVariant Identifiers: chr2:g.215645367G>A (hg19) ; chr2:g.214780643G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214780643G>A , CM000664.2:g.214780643G>A	GRCh38
NC_000002.11:g.215645367G>A , CM000664.1:g.215645367G>A	GRCh37
NC_000002.10:g.215353612G>A	NCBI36
NG_012047.2:g.34062C>T
NG_012047.3:g.34069C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.1231C>T MANE Select	ENSP00000260947.4:p.Pro411Ser
ENST00000421162.2:c.215+16418C>T	ENSP00000392245.2:n.215+16418C>T
ENST00000613192.2:c.158+28769C>T	ENSP00000483275.2:n.158+28769C>T
ENST00000613374.5:c.159-28088C>T	ENSP00000484464.1:n.159-28088C>T
ENST00000613706.5:c.906+325C>T	ENSP00000484976.2:n.906+325C>T
ENST00000617164.5:c.1174C>T	ENSP00000480470.1:p.Pro392Ser
ENST00000619009.5:c.364+11654C>T	ENSP00000482293.1:n.364+11654C>T
ENST00000650978.1:c.1073C>T
ENST00000260947.8:c.1231C>T	ENSP00000260947.4:p.Pro411Ser
ENST00000421162.1:c.215+16418C>T	ENSP00000392245.1:n.215+16418C>T
ENST00000455743.5:c.*851C>T	ENSP00000412186.1:n.*851C>T
ENST00000613192.1:c.73+28769C>T	ENSP00000483275.1:n.73+28769C>T
ENST00000613374.4:c.159-28088C>T	ENSP00000484464.1:n.159-28088C>T
ENST00000613706.4:c.215+16418C>T	ENSP00000484976.1:n.215+16418C>T
ENST00000617164.4:c.1174C>T	ENSP00000480470.1:p.Pro392Ser
ENST00000619009.4:c.364+11654C>T	ENSP00000482293.1:n.364+11654C>T
ENST00000620057.4:c.365-11331C>T	ENSP00000481988.1:n.365-11331C>T
NM_000465.3:c.1231C>T	NP_000456.2:p.Pro411Ser
NM_001282543.1:c.1174C>T	NP_001269472.1:p.Pro392Ser
NM_001282545.1:c.215+16418C>T	NP_001269474.1:n.215+16418C>T
NM_001282548.1:c.159-28088C>T	NP_001269477.1:n.159-28088C>T
NM_001282549.1:c.364+11654C>T	NP_001269478.1:n.364+11654C>T
NR_104212.1:n.1224C>T
NR_104215.1:n.1167C>T
NR_104216.1:n.507-11331C>T
XM_011511567.1:c.1177C>T	XP_011509869.1:p.Pro393Ser
XM_011511568.1:c.1231C>T	XP_011509870.1:p.Pro411Ser
XM_017004613.1:c.1330C>T	XP_016860102.1:p.Pro444Ser
XM_017004614.1:c.1330C>T	XP_016860103.1:p.Pro444Ser
XR_002959322.1:n.1421C>T
NM_000465.4:c.1231C>T MANE Select	NP_000456.2:p.Pro411Ser
NM_001282543.2:c.1174C>T	NP_001269472.1:p.Pro392Ser
NM_001282545.2:c.215+16418C>T	NP_001269474.1:n.215+16418C>T
NM_001282548.2:c.159-28088C>T	NP_001269477.1:n.159-28088C>T
NM_001282549.2:c.364+11654C>T	NP_001269478.1:n.364+11654C>T
NR_104212.2:n.1196C>T
NR_104215.2:n.1139C>T
NR_104216.2:n.479-11331C>T