Canonical Allele Identifier: CA2577234231

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214728650T>C , CM000664.2:g.214728650T>C	GRCh38
NC_000002.11:g.215593374T>C , CM000664.1:g.215593374T>C	GRCh37
NC_000002.10:g.215301619T>C	NCBI36
NG_012047.2:g.86055A>G
NG_012047.3:g.86062A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000260947.9:c.*26A>G MANE Select	ENSP00000260947.4:n.*26A>G
ENST00000613374.5:c.*26A>G	ENSP00000484464.1:n.*26A>G
ENST00000613706.5:c.*26A>G	ENSP00000484976.2:n.*26A>G
ENST00000617164.5:c.*26A>G	ENSP00000480470.1:n.*26A>G
ENST00000619009.5:c.*26A>G	ENSP00000482293.1:n.*26A>G
ENST00000650978.1:c.3735A>G
ENST00000260947.8:c.*26A>G	ENSP00000260947.4:n.*26A>G
ENST00000432456.5:c.503A>G
ENST00000471590.5:n.695A>G
ENST00000613374.4:c.*26A>G	ENSP00000484464.1:n.*26A>G
ENST00000613706.4:c.*26A>G	ENSP00000484976.1:n.*26A>G
ENST00000617164.4:c.*26A>G	ENSP00000480470.1:n.*26A>G
ENST00000619009.4:c.*26A>G	ENSP00000482293.1:n.*26A>G
NM_000465.3:c.*26A>G	NP_000456.2:n.*26A>G
NM_001282543.1:c.*26A>G	NP_001269472.1:n.*26A>G
NM_001282545.1:c.*26A>G	NP_001269474.1:n.*26A>G
NM_001282548.1:c.*26A>G	NP_001269477.1:n.*26A>G
NM_001282549.1:c.*26A>G	NP_001269478.1:n.*26A>G
NR_104212.1:n.2353A>G
NR_104215.1:n.2296A>G
NR_104216.1:n.1552A>G
XM_011511567.1:c.*26A>G	XP_011509869.1:n.*26A>G
XM_017004613.1:c.*26A>G	XP_016860102.1:n.*26A>G
XR_002959322.1:n.2726A>G
NM_000465.4:c.*26A>G MANE Select	NP_000456.2:n.*26A>G
NM_001282543.2:c.*26A>G	NP_001269472.1:n.*26A>G
NM_001282545.2:c.*26A>G	NP_001269474.1:n.*26A>G
NM_001282548.2:c.*26A>G	NP_001269477.1:n.*26A>G
NM_001282549.2:c.*26A>G	NP_001269478.1:n.*26A>G
NR_104212.2:n.2325A>G
NR_104215.2:n.2268A>G
NR_104216.2:n.1524A>G