Canonical Allele Identifier: CA2662971949

Gene: BARD1

Linked Data

• gnomAD v4: 2-214792149-T-TAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214792149_214792150insAAA , CM000664.2:g.214792149_214792150insAAA	GRCh38
NC_000002.11:g.215656873_215656874insAAA , CM000664.1:g.215656873_215656874insAAA	GRCh37
NC_000002.10:g.215365118_215365119insAAA	NCBI36
NG_012047.2:g.22555_22556insTTT
NG_012047.3:g.22562_22563insTTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000260947.9:c.364+147_364+148insTTT MANE Select	ENSP00000260947.4:n.364+147_364+148insTTT...
ENST00000421162.2:c.215+4911_215+4912insTTT	ENSP00000392245.2:n.215+4911_215+4912insT...
ENST00000613192.2:c.158+17262_158+17263insTTT	ENSP00000483275.2:n.158+17262_158+17263in...
ENST00000613374.5:c.158+17262_158+17263insTTT	ENSP00000484464.1:n.158+17262_158+17263in...
ENST00000613706.5:c.364+147_364+148insTTT	ENSP00000484976.2:n.364+147_364+148insTTT...
ENST00000617164.5:c.307+147_307+148insTTT	ENSP00000480470.1:n.307+147_307+148insTTT...
ENST00000619009.5:c.364+147_364+148insTTT	ENSP00000482293.1:n.364+147_364+148insTTT...
ENST00000650978.1:c.206+147_206+148insTTT
ENST00000260947.8:c.364+147_364+148insTTT	ENSP00000260947.4:n.364+147_364+148insTTT...
ENST00000421162.1:c.215+4911_215+4912insTTT	ENSP00000392245.1:n.215+4911_215+4912insT...
ENST00000455743.5:c.215+4911_215+4912insTTT	ENSP00000412186.1:n.215+4911_215+4912insT...
ENST00000471787.1:n.260-10641_260-10640insTTT
ENST00000613192.1:c.73+17262_73+17263insTTT	ENSP00000483275.1:n.73+17262_73+17263insT...
ENST00000613374.4:c.158+17262_158+17263insTTT	ENSP00000484464.1:n.158+17262_158+17263in...
ENST00000613706.4:c.215+4911_215+4912insTTT	ENSP00000484976.1:n.215+4911_215+4912insT...
ENST00000617164.4:c.307+147_307+148insTTT	ENSP00000480470.1:n.307+147_307+148insTTT...
ENST00000619009.4:c.364+147_364+148insTTT	ENSP00000482293.1:n.364+147_364+148insTTT...
ENST00000620057.4:c.364+147_364+148insTTT	ENSP00000481988.1:n.364+147_364+148insTTT...
NM_000465.3:c.364+147_364+148insTTT	NP_000456.2:n.364+147_364+148insTTT
NM_001282543.1:c.307+147_307+148insTTT	NP_001269472.1:n.307+147_307+148insTTT
NM_001282545.1:c.215+4911_215+4912insTTT	NP_001269474.1:n.215+4911_215+4912insTTT
NM_001282548.1:c.158+17262_158+17263insTTT	NP_001269477.1:n.158+17262_158+17263insTT...
NM_001282549.1:c.364+147_364+148insTTT	NP_001269478.1:n.364+147_364+148insTTT
NR_104212.1:n.357+4911_357+4912insTTT
NR_104215.1:n.301-10641_301-10640insTTT
NR_104216.1:n.506+147_506+148insTTT
XM_011511567.1:c.310+147_310+148insTTT	XP_011509869.1:n.310+147_310+148insTTT
XM_011511568.1:c.364+147_364+148insTTT	XP_011509870.1:n.364+147_364+148insTTT
XM_017004613.1:c.463+147_463+148insTTT	XP_016860102.1:n.463+147_463+148insTTT
XM_017004614.1:c.463+147_463+148insTTT	XP_016860103.1:n.463+147_463+148insTTT
XR_002959322.1:n.554+147_554+148insTTT
NM_000465.4:c.364+147_364+148insTTT MANE Select	NP_000456.2:n.364+147_364+148insTTT
NM_001282543.2:c.307+147_307+148insTTT	NP_001269472.1:n.307+147_307+148insTTT
NM_001282545.2:c.215+4911_215+4912insTTT	NP_001269474.1:n.215+4911_215+4912insTTT
NM_001282548.2:c.158+17262_158+17263insTTT	NP_001269477.1:n.158+17262_158+17263insTT...
NM_001282549.2:c.364+147_364+148insTTT	NP_001269478.1:n.364+147_364+148insTTT
NR_104212.2:n.329+4911_329+4912insTTT
NR_104215.2:n.273-10641_273-10640insTTT
NR_104216.2:n.478+147_478+148insTTT