Canonical Allele Identifier: CA1327046391

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214730462_214730463delinsCT , CM000664.2:g.214730462_214730463delinsCT	GRCh38
NC_000002.11:g.215595186_215595187delinsCT , CM000664.1:g.215595186_215595187delinsCT	GRCh37
NC_000002.10:g.215303431_215303432delinsCT	NCBI36
NG_012047.2:g.84242_84243delinsAG
NG_012047.3:g.84249_84250delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.1949_1950delinsAG MANE Select	ENSP00000260947.4:p.Lys650=
ENST00000421162.2:c.596_597delinsAG	ENSP00000392245.2:p.Lys199=
ENST00000613192.2:c.*12_*13delinsAG	ENSP00000483275.2:n.*12_*13delinsAG
ENST00000613374.5:c.539_540delinsAG	ENSP00000484464.1:p.Lys180=
ENST00000613706.5:c.1541_1542delinsAG	ENSP00000484976.2:p.Lys514=
ENST00000617164.5:c.1892_1893delinsAG	ENSP00000480470.1:p.Lys631=
ENST00000619009.5:c.410_411delinsAG	ENSP00000482293.1:p.Lys137=
ENST00000650978.1:c.3324_3325delinsAG
ENST00000260947.8:c.1949_1950delinsAG	ENSP00000260947.4:p.Lys650=
ENST00000421162.1:c.596_597delinsAG	ENSP00000392245.1:p.Lys199=
ENST00000432456.5:c.46_47delinsAG
ENST00000455743.5:c.*1569_*1570delinsAG	ENSP00000412186.1:n.*1569_*1570delinsAG
ENST00000471590.5:n.284_285delinsAG
ENST00000613192.1:c.119_120delinsAG	ENSP00000483275.1:p.Lys40=
ENST00000613374.4:c.539_540delinsAG	ENSP00000484464.1:p.Lys180=
ENST00000613706.4:c.596_597delinsAG	ENSP00000484976.1:p.Lys199=
ENST00000617164.4:c.1892_1893delinsAG	ENSP00000480470.1:p.Lys631=
ENST00000619009.4:c.410_411delinsAG	ENSP00000482293.1:p.Lys137=
ENST00000620057.4:c.*615_*616delinsAG	ENSP00000481988.1:n.*615_*616delinsAG
NM_000465.3:c.1949_1950delinsAG	NP_000456.2:p.Lys650=
NM_001282543.1:c.1892_1893delinsAG	NP_001269472.1:p.Lys631=
NM_001282545.1:c.596_597delinsAG	NP_001269474.1:p.Lys199=
NM_001282548.1:c.539_540delinsAG	NP_001269477.1:p.Lys180=
NM_001282549.1:c.410_411delinsAG	NP_001269478.1:p.Lys137=
NR_104212.1:n.1942_1943delinsAG
NR_104215.1:n.1885_1886delinsAG
NR_104216.1:n.1141_1142delinsAG
XM_011511567.1:c.1895_1896delinsAG	XP_011509869.1:p.Lys632=
XM_017004613.1:c.2048_2049delinsAG	XP_016860102.1:p.Lys683=
XR_002959322.1:n.2139_2140delinsAG
NM_000465.4:c.1949_1950delinsAG MANE Select	NP_000456.2:p.Lys650=
NM_001282543.2:c.1892_1893delinsAG	NP_001269472.1:p.Lys631=
NM_001282545.2:c.596_597delinsAG	NP_001269474.1:p.Lys199=
NM_001282548.2:c.539_540delinsAG	NP_001269477.1:p.Lys180=
NM_001282549.2:c.410_411delinsAG	NP_001269478.1:p.Lys137=
NR_104212.2:n.1914_1915delinsAG
NR_104215.2:n.1857_1858delinsAG
NR_104216.2:n.1113_1114delinsAG