Canonical Allele Identifier: CA350460973

Gene: BARD1

Linked Data

• COSMIC: COSM6316862 ; COSM6316863
• MyVariant Identifiers: chr2:g.215657079G>T (hg19) ; chr2:g.214792355G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214792355G>T , CM000664.2:g.214792355G>T	GRCh38
NC_000002.11:g.215657079G>T , CM000664.1:g.215657079G>T	GRCh37
NC_000002.10:g.215365324G>T	NCBI36
NG_012047.2:g.22350C>A
NG_012047.3:g.22357C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.306C>A MANE Select	ENSP00000260947.4:p.Asp102Glu
ENST00000421162.2:c.215+4706C>A	ENSP00000392245.2:n.215+4706C>A
ENST00000613192.2:c.158+17057C>A	ENSP00000483275.2:n.158+17057C>A
ENST00000613374.5:c.158+17057C>A	ENSP00000484464.1:n.158+17057C>A
ENST00000613706.5:c.306C>A	ENSP00000484976.2:p.Asp102Glu
ENST00000617164.5:c.249C>A	ENSP00000480470.1:p.Asp83Glu
ENST00000619009.5:c.306C>A	ENSP00000482293.1:p.Asp102Glu
ENST00000650978.1:c.148C>A
ENST00000260947.8:c.306C>A	ENSP00000260947.4:p.Asp102Glu
ENST00000421162.1:c.215+4706C>A	ENSP00000392245.1:n.215+4706C>A
ENST00000455743.5:c.215+4706C>A	ENSP00000412186.1:n.215+4706C>A
ENST00000471787.1:n.260-10846C>A
ENST00000613192.1:c.73+17057C>A	ENSP00000483275.1:n.73+17057C>A
ENST00000613374.4:c.158+17057C>A	ENSP00000484464.1:n.158+17057C>A
ENST00000613706.4:c.215+4706C>A	ENSP00000484976.1:n.215+4706C>A
ENST00000617164.4:c.249C>A	ENSP00000480470.1:p.Asp83Glu
ENST00000619009.4:c.306C>A	ENSP00000482293.1:p.Asp102Glu
ENST00000620057.4:c.306C>A	ENSP00000481988.1:p.Asp102Glu
NM_000465.3:c.306C>A	NP_000456.2:p.Asp102Glu
NM_001282543.1:c.249C>A	NP_001269472.1:p.Asp83Glu
NM_001282545.1:c.215+4706C>A	NP_001269474.1:n.215+4706C>A
NM_001282548.1:c.158+17057C>A	NP_001269477.1:n.158+17057C>A
NM_001282549.1:c.306C>A	NP_001269478.1:p.Asp102Glu
NR_104212.1:n.357+4706C>A
NR_104215.1:n.301-10846C>A
NR_104216.1:n.448C>A
XM_011511567.1:c.252C>A	XP_011509869.1:p.Asp84Glu
XM_011511568.1:c.306C>A	XP_011509870.1:p.Asp102Glu
XM_017004613.1:c.405C>A	XP_016860102.1:p.Asp135Glu
XM_017004614.1:c.405C>A	XP_016860103.1:p.Asp135Glu
XR_002959322.1:n.496C>A
NM_000465.4:c.306C>A MANE Select	NP_000456.2:p.Asp102Glu
NM_001282543.2:c.249C>A	NP_001269472.1:p.Asp83Glu
NM_001282545.2:c.215+4706C>A	NP_001269474.1:n.215+4706C>A
NM_001282548.2:c.158+17057C>A	NP_001269477.1:n.158+17057C>A
NM_001282549.2:c.306C>A	NP_001269478.1:p.Asp102Glu
NR_104212.2:n.329+4706C>A
NR_104215.2:n.273-10846C>A
NR_104216.2:n.420C>A