Canonical Allele Identifier: CA64802149

Gene: BARD1

Linked Data

• dbSNP Id: rs558856376
• MyVariant Identifiers: chr2:g.215609561_215609562insA (hg19) ; chr2:g.214744837_214744838insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214744838dup , CM000664.2:g.214744838dup	GRCh38
NC_000002.11:g.215609562dup , CM000664.1:g.215609562dup	GRCh37
NC_000002.10:g.215317807dup	NCBI36
NG_012047.2:g.69867dup
NG_012047.3:g.69874dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.1903+229dup MANE Select	ENSP00000260947.4:n.1903+229dup
ENST00000421162.2:c.550+229dup	ENSP00000392245.2:n.550+229dup
ENST00000613192.2:c.159-14330dup	ENSP00000483275.2:n.159-14330dup
ENST00000613374.5:c.493+229dup	ENSP00000484464.1:n.493+229dup
ENST00000613706.5:c.1495+229dup	ENSP00000484976.2:n.1495+229dup
ENST00000617164.5:c.1846+229dup	ENSP00000480470.1:n.1846+229dup
ENST00000619009.5:c.365-14330dup	ENSP00000482293.1:n.365-14330dup
ENST00000650978.1:c.3278+229dup
ENST00000260947.8:c.1903+229dup	ENSP00000260947.4:n.1903+229dup
ENST00000421162.1:c.550+229dup	ENSP00000392245.1:n.550+229dup
ENST00000455743.5:c.*1523+229dup	ENSP00000412186.1:n.*1523+229dup
ENST00000613192.1:c.74-14330dup	ENSP00000483275.1:n.74-14330dup
ENST00000613374.4:c.493+229dup	ENSP00000484464.1:n.493+229dup
ENST00000613706.4:c.550+229dup	ENSP00000484976.1:n.550+229dup
ENST00000617164.4:c.1846+229dup	ENSP00000480470.1:n.1846+229dup
ENST00000619009.4:c.365-14330dup	ENSP00000482293.1:n.365-14330dup
ENST00000620057.4:c.*569+229dup	ENSP00000481988.1:n.*569+229dup
NM_000465.3:c.1903+229dup	NP_000456.2:n.1903+229dup
NM_001282543.1:c.1846+229dup	NP_001269472.1:n.1846+229dup
NM_001282545.1:c.550+229dup	NP_001269474.1:n.550+229dup
NM_001282548.1:c.493+229dup	NP_001269477.1:n.493+229dup
NM_001282549.1:c.365-14330dup	NP_001269478.1:n.365-14330dup
NR_104212.1:n.1896+229dup
NR_104215.1:n.1839+229dup
NR_104216.1:n.1095+229dup
XM_011511567.1:c.1849+229dup	XP_011509869.1:n.1849+229dup
XM_011511568.1:c.1903+229dup	XP_011509870.1:n.1903+229dup
XM_017004613.1:c.2002+229dup	XP_016860102.1:n.2002+229dup
XM_017004614.1:c.2002+229dup	XP_016860103.1:n.2002+229dup
XR_002959322.1:n.2093+229dup
NM_000465.4:c.1903+229dup MANE Select	NP_000456.2:n.1903+229dup
NM_001282543.2:c.1846+229dup	NP_001269472.1:n.1846+229dup
NM_001282545.2:c.550+229dup	NP_001269474.1:n.550+229dup
NM_001282548.2:c.493+229dup	NP_001269477.1:n.493+229dup
NM_001282549.2:c.365-14330dup	NP_001269478.1:n.365-14330dup
NR_104212.2:n.1868+229dup
NR_104215.2:n.1811+229dup
NR_104216.2:n.1067+229dup