Canonical Allele Identifier: CA431390512

Gene: BARD1

Linked Data

• ClinVar Variation Id: 1636722
• ClinVar RCV Id: RCV002128580
• dbSNP Id: rs1057521964
• MyVariant Identifiers: chr2:g.215645536T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214780812T>G , CM000664.2:g.214780812T>G	GRCh38
NC_000002.11:g.215645536T>G , CM000664.1:g.215645536T>G	GRCh37
NC_000002.10:g.215353781T>G	NCBI36
NG_012047.2:g.33893A>C
NG_012047.3:g.33900A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.1062A>C MANE Select	ENSP00000260947.4:p.Ser354=
ENST00000421162.2:c.215+16249A>C	ENSP00000392245.2:n.215+16249A>C
ENST00000613192.2:c.158+28600A>C	ENSP00000483275.2:n.158+28600A>C
ENST00000613374.5:c.159-28257A>C	ENSP00000484464.1:n.159-28257A>C
ENST00000613706.5:c.906+156A>C	ENSP00000484976.2:n.906+156A>C
ENST00000617164.5:c.1005A>C	ENSP00000480470.1:p.Ser335=
ENST00000619009.5:c.364+11485A>C	ENSP00000482293.1:n.364+11485A>C
ENST00000650978.1:c.904A>C
ENST00000260947.8:c.1062A>C	ENSP00000260947.4:p.Ser354=
ENST00000421162.1:c.215+16249A>C	ENSP00000392245.1:n.215+16249A>C
ENST00000455743.5:c.*682A>C	ENSP00000412186.1:n.*682A>C
ENST00000613192.1:c.73+28600A>C	ENSP00000483275.1:n.73+28600A>C
ENST00000613374.4:c.159-28257A>C	ENSP00000484464.1:n.159-28257A>C
ENST00000613706.4:c.215+16249A>C	ENSP00000484976.1:n.215+16249A>C
ENST00000617164.4:c.1005A>C	ENSP00000480470.1:p.Ser335=
ENST00000619009.4:c.364+11485A>C	ENSP00000482293.1:n.364+11485A>C
ENST00000620057.4:c.364+11485A>C	ENSP00000481988.1:n.364+11485A>C
NM_000465.3:c.1062A>C	NP_000456.2:p.Ser354=
NM_001282543.1:c.1005A>C	NP_001269472.1:p.Ser335=
NM_001282545.1:c.215+16249A>C	NP_001269474.1:n.215+16249A>C
NM_001282548.1:c.159-28257A>C	NP_001269477.1:n.159-28257A>C
NM_001282549.1:c.364+11485A>C	NP_001269478.1:n.364+11485A>C
NR_104212.1:n.1055A>C
NR_104215.1:n.998A>C
NR_104216.1:n.506+11485A>C
XM_011511567.1:c.1008A>C	XP_011509869.1:p.Ser336=
XM_011511568.1:c.1062A>C	XP_011509870.1:p.Ser354=
XM_017004613.1:c.1161A>C	XP_016860102.1:p.Ser387=
XM_017004614.1:c.1161A>C	XP_016860103.1:p.Ser387=
XR_002959322.1:n.1252A>C
NM_000465.4:c.1062A>C MANE Select	NP_000456.2:p.Ser354=
NM_001282543.2:c.1005A>C	NP_001269472.1:p.Ser335=
NM_001282545.2:c.215+16249A>C	NP_001269474.1:n.215+16249A>C
NM_001282548.2:c.159-28257A>C	NP_001269477.1:n.159-28257A>C
NM_001282549.2:c.364+11485A>C	NP_001269478.1:n.364+11485A>C
NR_104212.2:n.1027A>C
NR_104215.2:n.970A>C
NR_104216.2:n.478+11485A>C