Canonical Allele Identifier: CA1327071395

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214781259_214781260delinsCT , CM000664.2:g.214781259_214781260delinsCT	GRCh38
NC_000002.11:g.215645983_215645984delinsCT , CM000664.1:g.215645983_215645984delinsCT	GRCh37
NC_000002.10:g.215354228_215354229delinsCT	NCBI36
NG_012047.2:g.33445_33446delinsAG
NG_012047.3:g.33452_33453delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.614_615delinsAG MANE Select	ENSP00000260947.4:p.Lys205=
ENST00000421162.2:c.215+15801_215+15802delinsAG	ENSP00000392245.2:n.215+15801_215+15802delinsAG
ENST00000613192.2:c.158+28152_158+28153delinsAG	ENSP00000483275.2:n.158+28152_158+28153delinsAG
ENST00000613374.5:c.158+28152_158+28153delinsAG	ENSP00000484464.1:n.158+28152_158+28153delinsAG
ENST00000613706.5:c.614_615delinsAG	ENSP00000484976.2:p.Lys205=
ENST00000617164.5:c.557_558delinsAG	ENSP00000480470.1:p.Lys186=
ENST00000619009.5:c.364+11037_364+11038delinsAG	ENSP00000482293.1:n.364+11037_364+11038delinsAG
ENST00000650978.1:c.456_457delinsAG
ENST00000260947.8:c.614_615delinsAG	ENSP00000260947.4:p.Lys205=
ENST00000421162.1:c.215+15801_215+15802delinsAG	ENSP00000392245.1:n.215+15801_215+15802delinsAG
ENST00000455743.5:c.*234_*235delinsAG	ENSP00000412186.1:n.*234_*235delinsAG
ENST00000471787.1:n.509_510delinsAG
ENST00000613192.1:c.73+28152_73+28153delinsAG	ENSP00000483275.1:n.73+28152_73+28153delinsAG
ENST00000613374.4:c.158+28152_158+28153delinsAG	ENSP00000484464.1:n.158+28152_158+28153delinsAG
ENST00000613706.4:c.215+15801_215+15802delinsAG	ENSP00000484976.1:n.215+15801_215+15802delinsAG
ENST00000617164.4:c.557_558delinsAG	ENSP00000480470.1:p.Lys186=
ENST00000619009.4:c.364+11037_364+11038delinsAG	ENSP00000482293.1:n.364+11037_364+11038delinsAG
ENST00000620057.4:c.364+11037_364+11038delinsAG	ENSP00000481988.1:n.364+11037_364+11038delinsAG
NM_000465.3:c.614_615delinsAG	NP_000456.2:p.Lys205=
NM_001282543.1:c.557_558delinsAG	NP_001269472.1:p.Lys186=
NM_001282545.1:c.215+15801_215+15802delinsAG	NP_001269474.1:n.215+15801_215+15802delinsAG
NM_001282548.1:c.158+28152_158+28153delinsAG	NP_001269477.1:n.158+28152_158+28153delinsAG
NM_001282549.1:c.364+11037_364+11038delinsAG	NP_001269478.1:n.364+11037_364+11038delinsAG
NR_104212.1:n.607_608delinsAG
NR_104215.1:n.550_551delinsAG
NR_104216.1:n.506+11037_506+11038delinsAG
XM_011511567.1:c.560_561delinsAG	XP_011509869.1:p.Lys187=
XM_011511568.1:c.614_615delinsAG	XP_011509870.1:p.Lys205=
XM_017004613.1:c.713_714delinsAG	XP_016860102.1:p.Lys238=
XM_017004614.1:c.713_714delinsAG	XP_016860103.1:p.Lys238=
XR_002959322.1:n.804_805delinsAG
NM_000465.4:c.614_615delinsAG MANE Select	NP_000456.2:p.Lys205=
NM_001282543.2:c.557_558delinsAG	NP_001269472.1:p.Lys186=
NM_001282545.2:c.215+15801_215+15802delinsAG	NP_001269474.1:n.215+15801_215+15802delinsAG
NM_001282548.2:c.158+28152_158+28153delinsAG	NP_001269477.1:n.158+28152_158+28153delinsAG
NM_001282549.2:c.364+11037_364+11038delinsAG	NP_001269478.1:n.364+11037_364+11038delinsAG
NR_104212.2:n.579_580delinsAG
NR_104215.2:n.522_523delinsAG
NR_104216.2:n.478+11037_478+11038delinsAG