Canonical Allele Identifier: CA2662971069

Gene: BARD1

Linked Data

• gnomAD v4: 2-214752667-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214752667_214752668insG , CM000664.2:g.214752667_214752668insG	GRCh38
NC_000002.11:g.215617391_215617392insG , CM000664.1:g.215617391_215617392insG	GRCh37
NC_000002.10:g.215325636_215325637insG	NCBI36
NG_012047.2:g.62037_62038insC
NG_012047.3:g.62044_62045insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.1569-113_1569-112insC MANE Select	ENSP00000260947.4:n.1569-113_1569-112insC
ENST00000421162.2:c.216-113_216-112insC	ENSP00000392245.2:n.216-113_216-112insC
ENST00000613192.2:c.159-22160_159-22159insC	ENSP00000483275.2:n.159-22160_159-22159insC
ENST00000613374.5:c.159-113_159-112insC	ENSP00000484464.1:n.159-113_159-112insC
ENST00000613706.5:c.1161-113_1161-112insC	ENSP00000484976.2:n.1161-113_1161-112insC
ENST00000617164.5:c.1512-113_1512-112insC	ENSP00000480470.1:n.1512-113_1512-112insC
ENST00000619009.5:c.365-22160_365-22159insC	ENSP00000482293.1:n.365-22160_365-22159insC
ENST00000650978.1:c.2944-113_2944-112insC
ENST00000260947.8:c.1569-113_1569-112insC	ENSP00000260947.4:n.1569-113_1569-112insC
ENST00000421162.1:c.216-113_216-112insC	ENSP00000392245.1:n.216-113_216-112insC
ENST00000455743.5:c.*1189-113_*1189-112insC	ENSP00000412186.1:n.*1189-113_*1189-112insC
ENST00000613192.1:c.74-22160_74-22159insC	ENSP00000483275.1:n.74-22160_74-22159insC
ENST00000613374.4:c.159-113_159-112insC	ENSP00000484464.1:n.159-113_159-112insC
ENST00000613706.4:c.216-113_216-112insC	ENSP00000484976.1:n.216-113_216-112insC
ENST00000617164.4:c.1512-113_1512-112insC	ENSP00000480470.1:n.1512-113_1512-112insC
ENST00000619009.4:c.365-22160_365-22159insC	ENSP00000482293.1:n.365-22160_365-22159insC
ENST00000620057.4:c.*235-113_*235-112insC	ENSP00000481988.1:n.*235-113_*235-112insC
NM_000465.3:c.1569-113_1569-112insC	NP_000456.2:n.1569-113_1569-112insC
NM_001282543.1:c.1512-113_1512-112insC	NP_001269472.1:n.1512-113_1512-112insC
NM_001282545.1:c.216-113_216-112insC	NP_001269474.1:n.216-113_216-112insC
NM_001282548.1:c.159-113_159-112insC	NP_001269477.1:n.159-113_159-112insC
NM_001282549.1:c.365-22160_365-22159insC	NP_001269478.1:n.365-22160_365-22159insC
NR_104212.1:n.1562-113_1562-112insC
NR_104215.1:n.1505-113_1505-112insC
NR_104216.1:n.761-113_761-112insC
XM_011511567.1:c.1515-113_1515-112insC	XP_011509869.1:n.1515-113_1515-112insC
XM_011511568.1:c.1569-113_1569-112insC	XP_011509870.1:n.1569-113_1569-112insC
XM_017004613.1:c.1668-113_1668-112insC	XP_016860102.1:n.1668-113_1668-112insC
XM_017004614.1:c.1668-113_1668-112insC	XP_016860103.1:n.1668-113_1668-112insC
XR_002959322.1:n.1759-113_1759-112insC
NM_000465.4:c.1569-113_1569-112insC MANE Select	NP_000456.2:n.1569-113_1569-112insC
NM_001282543.2:c.1512-113_1512-112insC	NP_001269472.1:n.1512-113_1512-112insC
NM_001282545.2:c.216-113_216-112insC	NP_001269474.1:n.216-113_216-112insC
NM_001282548.2:c.159-113_159-112insC	NP_001269477.1:n.159-113_159-112insC
NM_001282549.2:c.365-22160_365-22159insC	NP_001269478.1:n.365-22160_365-22159insC
NR_104212.2:n.1534-113_1534-112insC
NR_104215.2:n.1477-113_1477-112insC
NR_104216.2:n.733-113_733-112insC