Canonical Allele Identifier: CA2754202645

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214727996C>T , CM000664.2:g.214727996C>T	GRCh38
NC_000002.11:g.215592720C>T , CM000664.1:g.215592720C>T	GRCh37
NC_000002.10:g.215300965C>T	NCBI36
NG_012047.2:g.86709G>A
NG_012047.3:g.86716G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000260947.9:c.*680G>A MANE Select	ENSP00000260947.4:n.*680G>A
ENST00000260947.8:c.*680G>A	ENSP00000260947.4:n.*680G>A
ENST00000613374.4:c.*680G>A	ENSP00000484464.1:n.*680G>A
ENST00000613706.4:c.*680G>A	ENSP00000484976.1:n.*680G>A
ENST00000617164.4:c.*680G>A	ENSP00000480470.1:n.*680G>A
ENST00000619009.4:c.*680G>A	ENSP00000482293.1:n.*680G>A
NM_000465.3:c.*680G>A	NP_000456.2:n.*680G>A
NM_001282543.1:c.*680G>A	NP_001269472.1:n.*680G>A
NM_001282545.1:c.*680G>A	NP_001269474.1:n.*680G>A
NM_001282548.1:c.*680G>A	NP_001269477.1:n.*680G>A
NM_001282549.1:c.*680G>A	NP_001269478.1:n.*680G>A
NR_104212.1:n.3007G>A
NR_104215.1:n.2950G>A
NR_104216.1:n.2206G>A
XM_011511567.1:c.*680G>A	XP_011509869.1:n.*680G>A
XM_017004613.1:c.*680G>A	XP_016860102.1:n.*680G>A
NM_000465.4:c.*680G>A MANE Select	NP_000456.2:n.*680G>A
NM_001282543.2:c.*680G>A	NP_001269472.1:n.*680G>A
NM_001282545.2:c.*680G>A	NP_001269474.1:n.*680G>A
NM_001282548.2:c.*680G>A	NP_001269477.1:n.*680G>A
NM_001282549.2:c.*680G>A	NP_001269478.1:n.*680G>A
NR_104212.2:n.2979G>A
NR_104215.2:n.2922G>A
NR_104216.2:n.2178G>A