Canonical Allele Identifier: CA350456572

Gene: BARD1

Linked Data

• ClinVar Variation Id: 482781
• ClinVar RCV Id: RCV001858245
• dbSNP Id: rs1553622534
• MyVariant Identifiers: chr2:g.215645945C>T (hg19) ; chr2:g.214781221C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214781221C>T , CM000664.2:g.214781221C>T	GRCh38
NC_000002.11:g.215645945C>T , CM000664.1:g.215645945C>T	GRCh37
NC_000002.10:g.215354190C>T	NCBI36
NG_012047.2:g.33484G>A
NG_012047.3:g.33491G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000260947.9:c.653G>A MANE Select	ENSP00000260947.4:p.Trp218Ter
ENST00000421162.2:c.215+15840G>A	ENSP00000392245.2:n.215+15840G>A
ENST00000613192.2:c.158+28191G>A	ENSP00000483275.2:n.158+28191G>A
ENST00000613374.5:c.158+28191G>A	ENSP00000484464.1:n.158+28191G>A
ENST00000613706.5:c.653G>A	ENSP00000484976.2:p.Trp218Ter
ENST00000617164.5:c.596G>A	ENSP00000480470.1:p.Trp199Ter
ENST00000619009.5:c.364+11076G>A	ENSP00000482293.1:n.364+11076G>A
ENST00000650978.1:c.495G>A
ENST00000260947.8:c.653G>A	ENSP00000260947.4:p.Trp218Ter
ENST00000421162.1:c.215+15840G>A	ENSP00000392245.1:n.215+15840G>A
ENST00000455743.5:c.*273G>A	ENSP00000412186.1:n.*273G>A
ENST00000471787.1:n.548G>A
ENST00000613192.1:c.73+28191G>A	ENSP00000483275.1:n.73+28191G>A
ENST00000613374.4:c.158+28191G>A	ENSP00000484464.1:n.158+28191G>A
ENST00000613706.4:c.215+15840G>A	ENSP00000484976.1:n.215+15840G>A
ENST00000617164.4:c.596G>A	ENSP00000480470.1:p.Trp199Ter
ENST00000619009.4:c.364+11076G>A	ENSP00000482293.1:n.364+11076G>A
ENST00000620057.4:c.364+11076G>A	ENSP00000481988.1:n.364+11076G>A
NM_000465.3:c.653G>A	NP_000456.2:p.Trp218Ter
NM_001282543.1:c.596G>A	NP_001269472.1:p.Trp199Ter
NM_001282545.1:c.215+15840G>A	NP_001269474.1:n.215+15840G>A
NM_001282548.1:c.158+28191G>A	NP_001269477.1:n.158+28191G>A
NM_001282549.1:c.364+11076G>A	NP_001269478.1:n.364+11076G>A
NR_104212.1:n.646G>A
NR_104215.1:n.589G>A
NR_104216.1:n.506+11076G>A
XM_011511567.1:c.599G>A	XP_011509869.1:p.Trp200Ter
XM_011511568.1:c.653G>A	XP_011509870.1:p.Trp218Ter
XM_017004613.1:c.752G>A	XP_016860102.1:p.Trp251Ter
XM_017004614.1:c.752G>A	XP_016860103.1:p.Trp251Ter
XR_002959322.1:n.843G>A
NM_000465.4:c.653G>A MANE Select	NP_000456.2:p.Trp218Ter
NM_001282543.2:c.596G>A	NP_001269472.1:p.Trp199Ter
NM_001282545.2:c.215+15840G>A	NP_001269474.1:n.215+15840G>A
NM_001282548.2:c.158+28191G>A	NP_001269477.1:n.158+28191G>A
NM_001282549.2:c.364+11076G>A	NP_001269478.1:n.364+11076G>A
NR_104212.2:n.618G>A
NR_104215.2:n.561G>A
NR_104216.2:n.478+11076G>A