Canonical Allele Identifier: CA2566366978

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214809344_214809345insCGCG , CM000664.2:g.214809344_214809345insCGCG	GRCh38
NC_000002.11:g.215674068_215674069insCGCG , CM000664.1:g.215674068_215674069insCGCG	GRCh37
NC_000002.10:g.215382313_215382314insCGCG	NCBI36
NG_012047.2:g.5360_5361insCGCG
NG_012047.3:g.5367_5368insCGCG

Transcript Alleles

HGVS	Amino-acid change
ENST00000260947.9:c.158+67_158+68insCGCG MANE Select	ENSP00000260947.4:n.158+67_158+68insCGCG
ENST00000421162.2:c.158+67_158+68insCGCG	ENSP00000392245.2:n.158+67_158+68insCGCG
ENST00000613192.2:c.158+67_158+68insCGCG	ENSP00000483275.2:n.158+67_158+68insCGCG
ENST00000613374.5:c.158+67_158+68insCGCG	ENSP00000484464.1:n.158+67_158+68insCGCG
ENST00000613706.5:c.158+67_158+68insCGCG	ENSP00000484976.2:n.158+67_158+68insCGCG
ENST00000617164.5:c.158+67_158+68insCGCG	ENSP00000480470.1:n.158+67_158+68insCGCG
ENST00000619009.5:c.158+67_158+68insCGCG	ENSP00000482293.1:n.158+67_158+68insCGCG
ENST00000260947.8:c.158+67_158+68insCGCG	ENSP00000260947.4:n.158+67_158+68insCGCG
ENST00000421162.1:c.158+67_158+68insCGCG	ENSP00000392245.1:n.158+67_158+68insCGCG
ENST00000455743.5:c.158+67_158+68insCGCG	ENSP00000412186.1:n.158+67_158+68insCGCG
ENST00000471787.1:n.259+67_259+68insCGCG
ENST00000479904.1:n.249+67_249+68insCGCG
ENST00000613192.1:c.73+67_73+68insCGCG	ENSP00000483275.1:n.73+67_73+68insCGCG
ENST00000613374.4:c.158+67_158+68insCGCG	ENSP00000484464.1:n.158+67_158+68insCGCG
ENST00000613706.4:c.158+67_158+68insCGCG	ENSP00000484976.1:n.158+67_158+68insCGCG
ENST00000617164.4:c.158+67_158+68insCGCG	ENSP00000480470.1:n.158+67_158+68insCGCG
ENST00000619009.4:c.158+67_158+68insCGCG	ENSP00000482293.1:n.158+67_158+68insCGCG
ENST00000620057.4:c.158+67_158+68insCGCG	ENSP00000481988.1:n.158+67_158+68insCGCG
NM_000465.3:c.158+67_158+68insCGCG	NP_000456.2:n.158+67_158+68insCGCG
NM_001282543.1:c.158+67_158+68insCGCG	NP_001269472.1:n.158+67_158+68insCGCG
NM_001282545.1:c.158+67_158+68insCGCG	NP_001269474.1:n.158+67_158+68insCGCG
NM_001282548.1:c.158+67_158+68insCGCG	NP_001269477.1:n.158+67_158+68insCGCG
NM_001282549.1:c.158+67_158+68insCGCG	NP_001269478.1:n.158+67_158+68insCGCG
NR_104212.1:n.300+67_300+68insCGCG
NR_104215.1:n.300+67_300+68insCGCG
NR_104216.1:n.300+67_300+68insCGCG
XM_011511568.1:c.158+67_158+68insCGCG	XP_011509870.1:n.158+67_158+68insCGCG
XM_017004613.1:c.158+67_158+68insCGCG	XP_016860102.1:n.158+67_158+68insCGCG
XM_017004614.1:c.158+67_158+68insCGCG	XP_016860103.1:n.158+67_158+68insCGCG
XR_002959322.1:n.249+67_249+68insCGCG
NM_000465.4:c.158+67_158+68insCGCG MANE Select	NP_000456.2:n.158+67_158+68insCGCG
NM_001282543.2:c.158+67_158+68insCGCG	NP_001269472.1:n.158+67_158+68insCGCG
NM_001282545.2:c.158+67_158+68insCGCG	NP_001269474.1:n.158+67_158+68insCGCG
NM_001282548.2:c.158+67_158+68insCGCG	NP_001269477.1:n.158+67_158+68insCGCG
NM_001282549.2:c.158+67_158+68insCGCG	NP_001269478.1:n.158+67_158+68insCGCG
NR_104212.2:n.272+67_272+68insCGCG
NR_104215.2:n.272+67_272+68insCGCG
NR_104216.2:n.272+67_272+68insCGCG