Canonical Allele Identifier: CA10577822

Gene: BARD1

Linked Data

• ClinVar Variation Id: 231119
• ClinVar RCV Id: RCV000221465 ; RCV000703880 ; RCV000781928
• dbSNP Id: rs876658971
• gnomAD v3: 2-214780736-T-C
• gnomAD v4: 2-214780736-T-C
• MyVariant Identifiers: chr2:g.215645460T>C (hg19) ; chr2:g.214780736T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214780736T>C , CM000664.2:g.214780736T>C	GRCh38
NC_000002.11:g.215645460T>C , CM000664.1:g.215645460T>C	GRCh37
NC_000002.10:g.215353705T>C	NCBI36
NG_012047.2:g.33969A>G
NG_012047.3:g.33976A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000260947.9:c.1138A>G MANE Select	ENSP00000260947.4:p.Asn380Asp
ENST00000421162.2:c.215+16325A>G	ENSP00000392245.2:n.215+16325A>G
ENST00000613192.2:c.158+28676A>G	ENSP00000483275.2:n.158+28676A>G
ENST00000613374.5:c.159-28181A>G	ENSP00000484464.1:n.159-28181A>G
ENST00000613706.5:c.906+232A>G	ENSP00000484976.2:n.906+232A>G
ENST00000617164.5:c.1081A>G	ENSP00000480470.1:p.Asn361Asp
ENST00000619009.5:c.364+11561A>G	ENSP00000482293.1:n.364+11561A>G
ENST00000650978.1:c.980A>G
ENST00000260947.8:c.1138A>G	ENSP00000260947.4:p.Asn380Asp
ENST00000421162.1:c.215+16325A>G	ENSP00000392245.1:n.215+16325A>G
ENST00000455743.5:c.*758A>G	ENSP00000412186.1:n.*758A>G
ENST00000613192.1:c.73+28676A>G	ENSP00000483275.1:n.73+28676A>G
ENST00000613374.4:c.159-28181A>G	ENSP00000484464.1:n.159-28181A>G
ENST00000613706.4:c.215+16325A>G	ENSP00000484976.1:n.215+16325A>G
ENST00000617164.4:c.1081A>G	ENSP00000480470.1:p.Asn361Asp
ENST00000619009.4:c.364+11561A>G	ENSP00000482293.1:n.364+11561A>G
ENST00000620057.4:c.365-11424A>G	ENSP00000481988.1:n.365-11424A>G
NM_000465.3:c.1138A>G	NP_000456.2:p.Asn380Asp
NM_001282543.1:c.1081A>G	NP_001269472.1:p.Asn361Asp
NM_001282545.1:c.215+16325A>G	NP_001269474.1:n.215+16325A>G
NM_001282548.1:c.159-28181A>G	NP_001269477.1:n.159-28181A>G
NM_001282549.1:c.364+11561A>G	NP_001269478.1:n.364+11561A>G
NR_104212.1:n.1131A>G
NR_104215.1:n.1074A>G
NR_104216.1:n.507-11424A>G
XM_011511567.1:c.1084A>G	XP_011509869.1:p.Asn362Asp
XM_011511568.1:c.1138A>G	XP_011509870.1:p.Asn380Asp
XM_017004613.1:c.1237A>G	XP_016860102.1:p.Asn413Asp
XM_017004614.1:c.1237A>G	XP_016860103.1:p.Asn413Asp
XR_002959322.1:n.1328A>G
NM_000465.4:c.1138A>G MANE Select	NP_000456.2:p.Asn380Asp
NM_001282543.2:c.1081A>G	NP_001269472.1:p.Asn361Asp
NM_001282545.2:c.215+16325A>G	NP_001269474.1:n.215+16325A>G
NM_001282548.2:c.159-28181A>G	NP_001269477.1:n.159-28181A>G
NM_001282549.2:c.364+11561A>G	NP_001269478.1:n.364+11561A>G
NR_104212.2:n.1103A>G
NR_104215.2:n.1046A>G
NR_104216.2:n.479-11424A>G