Canonical Allele Identifier: CA287560

Gene: BARD1

Linked Data

• ClinVar Variation Id: 127749
• ClinVar RCV Id: RCV000226615 ; RCV000572061 ; RCV000656771 ; RCV001526799 ; RCV002307395
• dbSNP Id: rs200059956
• ExAC: 2:215645757 G / A
• gnomAD v2: 2-215645757-G-A
• gnomAD v3: 2-214781033-G-A
• gnomAD v4: 2-214781033-G-A
• COSMIC: COSM3673597 ; COSM3673598
• MyVariant Identifiers: chr2:g.215645757G>A (hg19) ; chr2:g.214781033G>A (hg38)
• PubMed: PMID:25980754 ; PMID:26976419 ; PMID:27978560

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214781033G>A , CM000664.2:g.214781033G>A	GRCh38
NC_000002.11:g.215645757G>A , CM000664.1:g.215645757G>A	GRCh37
NC_000002.10:g.215354002G>A	NCBI36
NG_012047.2:g.33672C>T
NG_012047.3:g.33679C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000260947.9:c.841C>T MANE Select	ENSP00000260947.4:p.Pro281Ser
ENST00000421162.2:c.215+16028C>T	ENSP00000392245.2:n.215+16028C>T
ENST00000613192.2:c.158+28379C>T	ENSP00000483275.2:n.158+28379C>T
ENST00000613374.5:c.158+28379C>T	ENSP00000484464.1:n.158+28379C>T
ENST00000613706.5:c.841C>T	ENSP00000484976.2:p.Pro281Ser
ENST00000617164.5:c.784C>T	ENSP00000480470.1:p.Pro262Ser
ENST00000619009.5:c.364+11264C>T	ENSP00000482293.1:n.364+11264C>T
ENST00000650978.1:c.683C>T
ENST00000260947.8:c.841C>T	ENSP00000260947.4:p.Pro281Ser
ENST00000421162.1:c.215+16028C>T	ENSP00000392245.1:n.215+16028C>T
ENST00000455743.5:c.*461C>T	ENSP00000412186.1:n.*461C>T
ENST00000471787.1:n.736C>T
ENST00000613192.1:c.73+28379C>T	ENSP00000483275.1:n.73+28379C>T
ENST00000613374.4:c.158+28379C>T	ENSP00000484464.1:n.158+28379C>T
ENST00000613706.4:c.215+16028C>T	ENSP00000484976.1:n.215+16028C>T
ENST00000617164.4:c.784C>T	ENSP00000480470.1:p.Pro262Ser
ENST00000619009.4:c.364+11264C>T	ENSP00000482293.1:n.364+11264C>T
ENST00000620057.4:c.364+11264C>T	ENSP00000481988.1:n.364+11264C>T
NM_000465.3:c.841C>T	NP_000456.2:p.Pro281Ser
NM_001282543.1:c.784C>T	NP_001269472.1:p.Pro262Ser
NM_001282545.1:c.215+16028C>T	NP_001269474.1:n.215+16028C>T
NM_001282548.1:c.158+28379C>T	NP_001269477.1:n.158+28379C>T
NM_001282549.1:c.364+11264C>T	NP_001269478.1:n.364+11264C>T
NR_104212.1:n.834C>T
NR_104215.1:n.777C>T
NR_104216.1:n.506+11264C>T
XM_011511567.1:c.787C>T	XP_011509869.1:p.Pro263Ser
XM_011511568.1:c.841C>T	XP_011509870.1:p.Pro281Ser
XM_017004613.1:c.940C>T	XP_016860102.1:p.Pro314Ser
XM_017004614.1:c.940C>T	XP_016860103.1:p.Pro314Ser
XR_002959322.1:n.1031C>T
NM_000465.4:c.841C>T MANE Select	NP_000456.2:p.Pro281Ser
NM_001282543.2:c.784C>T	NP_001269472.1:p.Pro262Ser
NM_001282545.2:c.215+16028C>T	NP_001269474.1:n.215+16028C>T
NM_001282548.2:c.158+28379C>T	NP_001269477.1:n.158+28379C>T
NM_001282549.2:c.364+11264C>T	NP_001269478.1:n.364+11264C>T
NR_104212.2:n.806C>T
NR_104215.2:n.749C>T
NR_104216.2:n.478+11264C>T