Canonical Allele Identifier: CA1327076806

Gene: BARD1

Linked Data

• dbSNP Id: rs1695578203
• gnomAD v3: 2-214792542-T-TC
• gnomAD v4: 2-214792542-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214792542_214792543insC , CM000664.2:g.214792542_214792543insC	GRCh38
NC_000002.11:g.215657266_215657267insC , CM000664.1:g.215657266_215657267insC	GRCh37
NC_000002.10:g.215365511_215365512insC	NCBI36
NG_012047.2:g.22162_22163insG
NG_012047.3:g.22169_22170insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.216-98_216-97insG MANE Select	ENSP00000260947.4:n.216-98_216-97insG
ENST00000421162.2:c.215+4518_215+4519insG	ENSP00000392245.2:n.215+4518_215+4519insG
ENST00000613192.2:c.158+16869_158+16870insG	ENSP00000483275.2:n.158+16869_158+16870insG
ENST00000613374.5:c.158+16869_158+16870insG	ENSP00000484464.1:n.158+16869_158+16870insG
ENST00000613706.5:c.216-98_216-97insG	ENSP00000484976.2:n.216-98_216-97insG
ENST00000617164.5:c.159-98_159-97insG	ENSP00000480470.1:n.159-98_159-97insG
ENST00000619009.5:c.216-98_216-97insG	ENSP00000482293.1:n.216-98_216-97insG
ENST00000650978.1:c.58-98_58-97insG
ENST00000260947.8:c.216-98_216-97insG	ENSP00000260947.4:n.216-98_216-97insG
ENST00000421162.1:c.215+4518_215+4519insG	ENSP00000392245.1:n.215+4518_215+4519insG
ENST00000455743.5:c.215+4518_215+4519insG	ENSP00000412186.1:n.215+4518_215+4519insG
ENST00000471787.1:n.260-11034_260-11033insG
ENST00000613192.1:c.73+16869_73+16870insG	ENSP00000483275.1:n.73+16869_73+16870insG
ENST00000613374.4:c.158+16869_158+16870insG	ENSP00000484464.1:n.158+16869_158+16870insG
ENST00000613706.4:c.215+4518_215+4519insG	ENSP00000484976.1:n.215+4518_215+4519insG
ENST00000617164.4:c.159-98_159-97insG	ENSP00000480470.1:n.159-98_159-97insG
ENST00000619009.4:c.216-98_216-97insG	ENSP00000482293.1:n.216-98_216-97insG
ENST00000620057.4:c.216-98_216-97insG	ENSP00000481988.1:n.216-98_216-97insG
NM_000465.3:c.216-98_216-97insG	NP_000456.2:n.216-98_216-97insG
NM_001282543.1:c.159-98_159-97insG	NP_001269472.1:n.159-98_159-97insG
NM_001282545.1:c.215+4518_215+4519insG	NP_001269474.1:n.215+4518_215+4519insG
NM_001282548.1:c.158+16869_158+16870insG	NP_001269477.1:n.158+16869_158+16870insG
NM_001282549.1:c.216-98_216-97insG	NP_001269478.1:n.216-98_216-97insG
NR_104212.1:n.357+4518_357+4519insG
NR_104215.1:n.301-11034_301-11033insG
NR_104216.1:n.358-98_358-97insG
XM_011511567.1:c.162-98_162-97insG	XP_011509869.1:n.162-98_162-97insG
XM_011511568.1:c.216-98_216-97insG	XP_011509870.1:n.216-98_216-97insG
XM_017004613.1:c.315-98_315-97insG	XP_016860102.1:n.315-98_315-97insG
XM_017004614.1:c.315-98_315-97insG	XP_016860103.1:n.315-98_315-97insG
XR_002959322.1:n.406-98_406-97insG
NM_000465.4:c.216-98_216-97insG MANE Select	NP_000456.2:n.216-98_216-97insG
NM_001282543.2:c.159-98_159-97insG	NP_001269472.1:n.159-98_159-97insG
NM_001282545.2:c.215+4518_215+4519insG	NP_001269474.1:n.215+4518_215+4519insG
NM_001282548.2:c.158+16869_158+16870insG	NP_001269477.1:n.158+16869_158+16870insG
NM_001282549.2:c.216-98_216-97insG	NP_001269478.1:n.216-98_216-97insG
NR_104212.2:n.329+4518_329+4519insG
NR_104215.2:n.273-11034_273-11033insG
NR_104216.2:n.330-98_330-97insG