Canonical Allele Identifier: CA2562269073

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214809366_214809367insCCG , CM000664.2:g.214809366_214809367insCCG	GRCh38
NC_000002.11:g.215674090_215674091insCCG , CM000664.1:g.215674090_215674091insCCG	GRCh37
NC_000002.10:g.215382335_215382336insCCG	NCBI36
NG_012047.2:g.5338_5339insCGG
NG_012047.3:g.5345_5346insCGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000260947.9:c.158+45_158+46insCGG MANE Select	ENSP00000260947.4:n.158+45_158+46insCGG
ENST00000421162.2:c.158+45_158+46insCGG	ENSP00000392245.2:n.158+45_158+46insCGG
ENST00000613192.2:c.158+45_158+46insCGG	ENSP00000483275.2:n.158+45_158+46insCGG
ENST00000613374.5:c.158+45_158+46insCGG	ENSP00000484464.1:n.158+45_158+46insCGG
ENST00000613706.5:c.158+45_158+46insCGG	ENSP00000484976.2:n.158+45_158+46insCGG
ENST00000617164.5:c.158+45_158+46insCGG	ENSP00000480470.1:n.158+45_158+46insCGG
ENST00000619009.5:c.158+45_158+46insCGG	ENSP00000482293.1:n.158+45_158+46insCGG
ENST00000260947.8:c.158+45_158+46insCGG	ENSP00000260947.4:n.158+45_158+46insCGG
ENST00000421162.1:c.158+45_158+46insCGG	ENSP00000392245.1:n.158+45_158+46insCGG
ENST00000455743.5:c.158+45_158+46insCGG	ENSP00000412186.1:n.158+45_158+46insCGG
ENST00000471787.1:n.259+45_259+46insCGG
ENST00000479904.1:n.249+45_249+46insCGG
ENST00000613192.1:c.73+45_73+46insCGG	ENSP00000483275.1:n.73+45_73+46insCGG
ENST00000613374.4:c.158+45_158+46insCGG	ENSP00000484464.1:n.158+45_158+46insCGG
ENST00000613706.4:c.158+45_158+46insCGG	ENSP00000484976.1:n.158+45_158+46insCGG
ENST00000617164.4:c.158+45_158+46insCGG	ENSP00000480470.1:n.158+45_158+46insCGG
ENST00000619009.4:c.158+45_158+46insCGG	ENSP00000482293.1:n.158+45_158+46insCGG
ENST00000620057.4:c.158+45_158+46insCGG	ENSP00000481988.1:n.158+45_158+46insCGG
NM_000465.3:c.158+45_158+46insCGG	NP_000456.2:n.158+45_158+46insCGG
NM_001282543.1:c.158+45_158+46insCGG	NP_001269472.1:n.158+45_158+46insCGG
NM_001282545.1:c.158+45_158+46insCGG	NP_001269474.1:n.158+45_158+46insCGG
NM_001282548.1:c.158+45_158+46insCGG	NP_001269477.1:n.158+45_158+46insCGG
NM_001282549.1:c.158+45_158+46insCGG	NP_001269478.1:n.158+45_158+46insCGG
NR_104212.1:n.300+45_300+46insCGG
NR_104215.1:n.300+45_300+46insCGG
NR_104216.1:n.300+45_300+46insCGG
XM_011511568.1:c.158+45_158+46insCGG	XP_011509870.1:n.158+45_158+46insCGG
XM_017004613.1:c.158+45_158+46insCGG	XP_016860102.1:n.158+45_158+46insCGG
XM_017004614.1:c.158+45_158+46insCGG	XP_016860103.1:n.158+45_158+46insCGG
XR_002959322.1:n.249+45_249+46insCGG
NM_000465.4:c.158+45_158+46insCGG MANE Select	NP_000456.2:n.158+45_158+46insCGG
NM_001282543.2:c.158+45_158+46insCGG	NP_001269472.1:n.158+45_158+46insCGG
NM_001282545.2:c.158+45_158+46insCGG	NP_001269474.1:n.158+45_158+46insCGG
NM_001282548.2:c.158+45_158+46insCGG	NP_001269477.1:n.158+45_158+46insCGG
NM_001282549.2:c.158+45_158+46insCGG	NP_001269478.1:n.158+45_158+46insCGG
NR_104212.2:n.272+45_272+46insCGG
NR_104215.2:n.272+45_272+46insCGG
NR_104216.2:n.272+45_272+46insCGG