Canonical Allele Identifier: CA350455083

Gene: BARD1

Linked Data

• ClinVar Variation Id: 920579
• ClinVar RCV Id: RCV001179428
• dbSNP Id: rs1326117428
• gnomAD v3: 2-214780957-T-G
• gnomAD v4: 2-214780957-T-G
• MyVariant Identifiers: chr2:g.215645681T>G (hg19) ; chr2:g.214780957T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214780957T>G , CM000664.2:g.214780957T>G	GRCh38
NC_000002.11:g.215645681T>G , CM000664.1:g.215645681T>G	GRCh37
NC_000002.10:g.215353926T>G	NCBI36
NG_012047.2:g.33748A>C
NG_012047.3:g.33755A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.917A>C MANE Select	ENSP00000260947.4:p.Asn306Thr
ENST00000421162.2:c.215+16104A>C	ENSP00000392245.2:n.215+16104A>C
ENST00000613192.2:c.158+28455A>C	ENSP00000483275.2:n.158+28455A>C
ENST00000613374.5:c.159-28402A>C	ENSP00000484464.1:n.159-28402A>C
ENST00000613706.5:c.906+11A>C	ENSP00000484976.2:n.906+11A>C
ENST00000617164.5:c.860A>C	ENSP00000480470.1:p.Asn287Thr
ENST00000619009.5:c.364+11340A>C	ENSP00000482293.1:n.364+11340A>C
ENST00000650978.1:c.759A>C
ENST00000260947.8:c.917A>C	ENSP00000260947.4:p.Asn306Thr
ENST00000421162.1:c.215+16104A>C	ENSP00000392245.1:n.215+16104A>C
ENST00000455743.5:c.*537A>C	ENSP00000412186.1:n.*537A>C
ENST00000471787.1:n.812A>C
ENST00000613192.1:c.73+28455A>C	ENSP00000483275.1:n.73+28455A>C
ENST00000613374.4:c.159-28402A>C	ENSP00000484464.1:n.159-28402A>C
ENST00000613706.4:c.215+16104A>C	ENSP00000484976.1:n.215+16104A>C
ENST00000617164.4:c.860A>C	ENSP00000480470.1:p.Asn287Thr
ENST00000619009.4:c.364+11340A>C	ENSP00000482293.1:n.364+11340A>C
ENST00000620057.4:c.364+11340A>C	ENSP00000481988.1:n.364+11340A>C
NM_000465.3:c.917A>C	NP_000456.2:p.Asn306Thr
NM_001282543.1:c.860A>C	NP_001269472.1:p.Asn287Thr
NM_001282545.1:c.215+16104A>C	NP_001269474.1:n.215+16104A>C
NM_001282548.1:c.159-28402A>C	NP_001269477.1:n.159-28402A>C
NM_001282549.1:c.364+11340A>C	NP_001269478.1:n.364+11340A>C
NR_104212.1:n.910A>C
NR_104215.1:n.853A>C
NR_104216.1:n.506+11340A>C
XM_011511567.1:c.863A>C	XP_011509869.1:p.Asn288Thr
XM_011511568.1:c.917A>C	XP_011509870.1:p.Asn306Thr
XM_017004613.1:c.1016A>C	XP_016860102.1:p.Asn339Thr
XM_017004614.1:c.1016A>C	XP_016860103.1:p.Asn339Thr
XR_002959322.1:n.1107A>C
NM_000465.4:c.917A>C MANE Select	NP_000456.2:p.Asn306Thr
NM_001282543.2:c.860A>C	NP_001269472.1:p.Asn287Thr
NM_001282545.2:c.215+16104A>C	NP_001269474.1:n.215+16104A>C
NM_001282548.2:c.159-28402A>C	NP_001269477.1:n.159-28402A>C
NM_001282549.2:c.364+11340A>C	NP_001269478.1:n.364+11340A>C
NR_104212.2:n.882A>C
NR_104215.2:n.825A>C
NR_104216.2:n.478+11340A>C