Canonical Allele Identifier: CA10584184

Gene: BARD1

Linked Data

• ClinVar Variation Id: 246176
• ClinVar RCV Id: RCV000235953 ; RCV000552182 ; RCV000565922 ; RCV000587901
• dbSNP Id: rs879254139
• gnomAD v4: 2-214797118-C-A
• MyVariant Identifiers: chr2:g.215661842C>A (hg19) ; chr2:g.214797118C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214797118C>A , CM000664.2:g.214797118C>A	GRCh38
NC_000002.11:g.215661842C>A , CM000664.1:g.215661842C>A	GRCh37
NC_000002.10:g.215370087C>A	NCBI36
NG_012047.2:g.17587G>T
NG_012047.3:g.17594G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.159-1G>T MANE Select	ENSP00000260947.4:n.159-1G>T
ENST00000421162.2:c.159-1G>T	ENSP00000392245.2:n.159-1G>T
ENST00000613192.2:c.158+12294G>T	ENSP00000483275.2:n.158+12294G>T
ENST00000613374.5:c.158+12294G>T	ENSP00000484464.1:n.158+12294G>T
ENST00000613706.5:c.159-1G>T	ENSP00000484976.2:n.159-1G>T
ENST00000617164.5:c.159-4673G>T	ENSP00000480470.1:n.159-4673G>T
ENST00000619009.5:c.159-1G>T	ENSP00000482293.1:n.159-1G>T
ENST00000260947.8:c.159-1G>T	ENSP00000260947.4:n.159-1G>T
ENST00000421162.1:c.159-1G>T	ENSP00000392245.1:n.159-1G>T
ENST00000455743.5:c.159-1G>T	ENSP00000412186.1:n.159-1G>T
ENST00000471787.1:n.259+12294G>T
ENST00000479904.1:n.250-1G>T
ENST00000613192.1:c.73+12294G>T	ENSP00000483275.1:n.73+12294G>T
ENST00000613374.4:c.158+12294G>T	ENSP00000484464.1:n.158+12294G>T
ENST00000613706.4:c.159-1G>T	ENSP00000484976.1:n.159-1G>T
ENST00000617164.4:c.159-4673G>T	ENSP00000480470.1:n.159-4673G>T
ENST00000619009.4:c.159-1G>T	ENSP00000482293.1:n.159-1G>T
ENST00000620057.4:c.159-1G>T	ENSP00000481988.1:n.159-1G>T
NM_000465.3:c.159-1G>T	NP_000456.2:n.159-1G>T
NM_001282543.1:c.159-4673G>T	NP_001269472.1:n.159-4673G>T
NM_001282545.1:c.159-1G>T	NP_001269474.1:n.159-1G>T
NM_001282548.1:c.158+12294G>T	NP_001269477.1:n.158+12294G>T
NM_001282549.1:c.159-1G>T	NP_001269478.1:n.159-1G>T
NR_104212.1:n.301-1G>T
NR_104215.1:n.300+12294G>T
NR_104216.1:n.301-1G>T
XM_011511567.1:c.105-1G>T	XP_011509869.1:n.105-1G>T
XM_011511568.1:c.159-1G>T	XP_011509870.1:n.159-1G>T
XM_017004613.1:c.159-1G>T	XP_016860102.1:n.159-1G>T
XM_017004614.1:c.159-1G>T	XP_016860103.1:n.159-1G>T
XR_002959322.1:n.250-1G>T
NM_000465.4:c.159-1G>T MANE Select	NP_000456.2:n.159-1G>T
NM_001282543.2:c.159-4673G>T	NP_001269472.1:n.159-4673G>T
NM_001282545.2:c.159-1G>T	NP_001269474.1:n.159-1G>T
NM_001282548.2:c.158+12294G>T	NP_001269477.1:n.158+12294G>T
NM_001282549.2:c.159-1G>T	NP_001269478.1:n.159-1G>T
NR_104212.2:n.273-1G>T
NR_104215.2:n.272+12294G>T
NR_104216.2:n.273-1G>T