Canonical Allele Identifier: CA350455002

Gene: BARD1

Linked Data

• ClinVar Variation Id: 489678
• ClinVar RCV Id: RCV000580385
• dbSNP Id: rs1553622340
• MyVariant Identifiers: chr2:g.215645669G>T (hg19) ; chr2:g.214780945G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214780945G>T , CM000664.2:g.214780945G>T	GRCh38
NC_000002.11:g.215645669G>T , CM000664.1:g.215645669G>T	GRCh37
NC_000002.10:g.215353914G>T	NCBI36
NG_012047.2:g.33760C>A
NG_012047.3:g.33767C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000260947.9:c.929C>A MANE Select	ENSP00000260947.4:p.Ser310Tyr
ENST00000421162.2:c.215+16116C>A	ENSP00000392245.2:n.215+16116C>A
ENST00000613192.2:c.158+28467C>A	ENSP00000483275.2:n.158+28467C>A
ENST00000613374.5:c.159-28390C>A	ENSP00000484464.1:n.159-28390C>A
ENST00000613706.5:c.906+23C>A	ENSP00000484976.2:n.906+23C>A
ENST00000617164.5:c.872C>A	ENSP00000480470.1:p.Ser291Tyr
ENST00000619009.5:c.364+11352C>A	ENSP00000482293.1:n.364+11352C>A
ENST00000650978.1:c.771C>A
ENST00000260947.8:c.929C>A	ENSP00000260947.4:p.Ser310Tyr
ENST00000421162.1:c.215+16116C>A	ENSP00000392245.1:n.215+16116C>A
ENST00000455743.5:c.*549C>A	ENSP00000412186.1:n.*549C>A
ENST00000471787.1:n.824C>A
ENST00000613192.1:c.73+28467C>A	ENSP00000483275.1:n.73+28467C>A
ENST00000613374.4:c.159-28390C>A	ENSP00000484464.1:n.159-28390C>A
ENST00000613706.4:c.215+16116C>A	ENSP00000484976.1:n.215+16116C>A
ENST00000617164.4:c.872C>A	ENSP00000480470.1:p.Ser291Tyr
ENST00000619009.4:c.364+11352C>A	ENSP00000482293.1:n.364+11352C>A
ENST00000620057.4:c.364+11352C>A	ENSP00000481988.1:n.364+11352C>A
NM_000465.3:c.929C>A	NP_000456.2:p.Ser310Tyr
NM_001282543.1:c.872C>A	NP_001269472.1:p.Ser291Tyr
NM_001282545.1:c.215+16116C>A	NP_001269474.1:n.215+16116C>A
NM_001282548.1:c.159-28390C>A	NP_001269477.1:n.159-28390C>A
NM_001282549.1:c.364+11352C>A	NP_001269478.1:n.364+11352C>A
NR_104212.1:n.922C>A
NR_104215.1:n.865C>A
NR_104216.1:n.506+11352C>A
XM_011511567.1:c.875C>A	XP_011509869.1:p.Ser292Tyr
XM_011511568.1:c.929C>A	XP_011509870.1:p.Ser310Tyr
XM_017004613.1:c.1028C>A	XP_016860102.1:p.Ser343Tyr
XM_017004614.1:c.1028C>A	XP_016860103.1:p.Ser343Tyr
XR_002959322.1:n.1119C>A
NM_000465.4:c.929C>A MANE Select	NP_000456.2:p.Ser310Tyr
NM_001282543.2:c.872C>A	NP_001269472.1:p.Ser291Tyr
NM_001282545.2:c.215+16116C>A	NP_001269474.1:n.215+16116C>A
NM_001282548.2:c.159-28390C>A	NP_001269477.1:n.159-28390C>A
NM_001282549.2:c.364+11352C>A	NP_001269478.1:n.364+11352C>A
NR_104212.2:n.894C>A
NR_104215.2:n.837C>A
NR_104216.2:n.478+11352C>A