Canonical Allele Identifier: CA1327070969

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214780663_214780664delinsTA , CM000664.2:g.214780663_214780664delinsTA	GRCh38
NC_000002.11:g.215645387_215645388delinsTA , CM000664.1:g.215645387_215645388delinsTA	GRCh37
NC_000002.10:g.215353632_215353633delinsTA	NCBI36
NG_012047.2:g.34041_34042delinsTA
NG_012047.3:g.34048_34049delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.1210_1211delinsTA MANE Select	ENSP00000260947.4:p.Tyr404=
ENST00000421162.2:c.215+16397_215+16398delinsTA	ENSP00000392245.2:n.215+16397_215+16398delinsTA
ENST00000613192.2:c.158+28748_158+28749delinsTA	ENSP00000483275.2:n.158+28748_158+28749delinsTA
ENST00000613374.5:c.159-28109_159-28108delinsTA	ENSP00000484464.1:n.159-28109_159-28108delinsTA
ENST00000613706.5:c.906+304_906+305delinsTA	ENSP00000484976.2:n.906+304_906+305delinsTA
ENST00000617164.5:c.1153_1154delinsTA	ENSP00000480470.1:p.Tyr385=
ENST00000619009.5:c.364+11633_364+11634delinsTA	ENSP00000482293.1:n.364+11633_364+11634delinsTA
ENST00000650978.1:c.1052_1053delinsTA
ENST00000260947.8:c.1210_1211delinsTA	ENSP00000260947.4:p.Tyr404=
ENST00000421162.1:c.215+16397_215+16398delinsTA	ENSP00000392245.1:n.215+16397_215+16398delinsTA
ENST00000455743.5:c.*830_*831delinsTA	ENSP00000412186.1:n.*830_*831delinsTA
ENST00000613192.1:c.73+28748_73+28749delinsTA	ENSP00000483275.1:n.73+28748_73+28749delinsTA
ENST00000613374.4:c.159-28109_159-28108delinsTA	ENSP00000484464.1:n.159-28109_159-28108delinsTA
ENST00000613706.4:c.215+16397_215+16398delinsTA	ENSP00000484976.1:n.215+16397_215+16398delinsTA
ENST00000617164.4:c.1153_1154delinsTA	ENSP00000480470.1:p.Tyr385=
ENST00000619009.4:c.364+11633_364+11634delinsTA	ENSP00000482293.1:n.364+11633_364+11634delinsTA
ENST00000620057.4:c.365-11352_365-11351delinsTA	ENSP00000481988.1:n.365-11352_365-11351delinsTA
NM_000465.3:c.1210_1211delinsTA	NP_000456.2:p.Tyr404=
NM_001282543.1:c.1153_1154delinsTA	NP_001269472.1:p.Tyr385=
NM_001282545.1:c.215+16397_215+16398delinsTA	NP_001269474.1:n.215+16397_215+16398delinsTA
NM_001282548.1:c.159-28109_159-28108delinsTA	NP_001269477.1:n.159-28109_159-28108delinsTA
NM_001282549.1:c.364+11633_364+11634delinsTA	NP_001269478.1:n.364+11633_364+11634delinsTA
NR_104212.1:n.1203_1204delinsTA
NR_104215.1:n.1146_1147delinsTA
NR_104216.1:n.507-11352_507-11351delinsTA
XM_011511567.1:c.1156_1157delinsTA	XP_011509869.1:p.Tyr386=
XM_011511568.1:c.1210_1211delinsTA	XP_011509870.1:p.Tyr404=
XM_017004613.1:c.1309_1310delinsTA	XP_016860102.1:p.Tyr437=
XM_017004614.1:c.1309_1310delinsTA	XP_016860103.1:p.Tyr437=
XR_002959322.1:n.1400_1401delinsTA
NM_000465.4:c.1210_1211delinsTA MANE Select	NP_000456.2:p.Tyr404=
NM_001282543.2:c.1153_1154delinsTA	NP_001269472.1:p.Tyr385=
NM_001282545.2:c.215+16397_215+16398delinsTA	NP_001269474.1:n.215+16397_215+16398delinsTA
NM_001282548.2:c.159-28109_159-28108delinsTA	NP_001269477.1:n.159-28109_159-28108delinsTA
NM_001282549.2:c.364+11633_364+11634delinsTA	NP_001269478.1:n.364+11633_364+11634delinsTA
NR_104212.2:n.1175_1176delinsTA
NR_104215.2:n.1118_1119delinsTA
NR_104216.2:n.479-11352_479-11351delinsTA