Canonical Allele Identifier: CA350461313

Gene: BARD1

Linked Data

• dbSNP Id: rs1574839978
• gnomAD v3: 2-214792432-C-A
• gnomAD v4: 2-214792432-C-A
• MyVariant Identifiers: chr2:g.215657156C>A (hg19) ; chr2:g.214792432C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214792432C>A , CM000664.2:g.214792432C>A	GRCh38
NC_000002.11:g.215657156C>A , CM000664.1:g.215657156C>A	GRCh37
NC_000002.10:g.215365401C>A	NCBI36
NG_012047.2:g.22273G>T
NG_012047.3:g.22280G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.229G>T MANE Select	ENSP00000260947.4:p.Asp77Tyr
ENST00000421162.2:c.215+4629G>T	ENSP00000392245.2:n.215+4629G>T
ENST00000613192.2:c.158+16980G>T	ENSP00000483275.2:n.158+16980G>T
ENST00000613374.5:c.158+16980G>T	ENSP00000484464.1:n.158+16980G>T
ENST00000613706.5:c.229G>T	ENSP00000484976.2:p.Asp77Tyr
ENST00000617164.5:c.172G>T	ENSP00000480470.1:p.Asp58Tyr
ENST00000619009.5:c.229G>T	ENSP00000482293.1:p.Asp77Tyr
ENST00000650978.1:c.71G>T
ENST00000260947.8:c.229G>T	ENSP00000260947.4:p.Asp77Tyr
ENST00000421162.1:c.215+4629G>T	ENSP00000392245.1:n.215+4629G>T
ENST00000455743.5:c.215+4629G>T	ENSP00000412186.1:n.215+4629G>T
ENST00000471787.1:n.260-10923G>T
ENST00000613192.1:c.73+16980G>T	ENSP00000483275.1:n.73+16980G>T
ENST00000613374.4:c.158+16980G>T	ENSP00000484464.1:n.158+16980G>T
ENST00000613706.4:c.215+4629G>T	ENSP00000484976.1:n.215+4629G>T
ENST00000617164.4:c.172G>T	ENSP00000480470.1:p.Asp58Tyr
ENST00000619009.4:c.229G>T	ENSP00000482293.1:p.Asp77Tyr
ENST00000620057.4:c.229G>T	ENSP00000481988.1:p.Asp77Tyr
NM_000465.3:c.229G>T	NP_000456.2:p.Asp77Tyr
NM_001282543.1:c.172G>T	NP_001269472.1:p.Asp58Tyr
NM_001282545.1:c.215+4629G>T	NP_001269474.1:n.215+4629G>T
NM_001282548.1:c.158+16980G>T	NP_001269477.1:n.158+16980G>T
NM_001282549.1:c.229G>T	NP_001269478.1:p.Asp77Tyr
NR_104212.1:n.357+4629G>T
NR_104215.1:n.301-10923G>T
NR_104216.1:n.371G>T
XM_011511567.1:c.175G>T	XP_011509869.1:p.Asp59Tyr
XM_011511568.1:c.229G>T	XP_011509870.1:p.Asp77Tyr
XM_017004613.1:c.328G>T	XP_016860102.1:p.Asp110Tyr
XM_017004614.1:c.328G>T	XP_016860103.1:p.Asp110Tyr
XR_002959322.1:n.419G>T
NM_000465.4:c.229G>T MANE Select	NP_000456.2:p.Asp77Tyr
NM_001282543.2:c.172G>T	NP_001269472.1:p.Asp58Tyr
NM_001282545.2:c.215+4629G>T	NP_001269474.1:n.215+4629G>T
NM_001282548.2:c.158+16980G>T	NP_001269477.1:n.158+16980G>T
NM_001282549.2:c.229G>T	NP_001269478.1:p.Asp77Tyr
NR_104212.2:n.329+4629G>T
NR_104215.2:n.273-10923G>T
NR_104216.2:n.343G>T