Canonical Allele Identifier: CA2662960695

Gene: BARD1

Linked Data

• gnomAD v4: 2-214780489-TCAAAAACTGCA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214780490_214780500del , CM000664.2:g.214780490_214780500del	GRCh38
NC_000002.11:g.215645214_215645224del , CM000664.1:g.215645214_215645224del	GRCh37
NC_000002.10:g.215353459_215353469del	NCBI36
NG_012047.2:g.34205_34215del
NG_012047.3:g.34212_34222del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.1314+60_1314+70del MANE Select	ENSP00000260947.4:n.1314+60_1314+70del
ENST00000421162.2:c.215+16561_215+16571del	ENSP00000392245.2:n.215+16561_215+16571del
ENST00000613192.2:c.158+28912_158+28922del	ENSP00000483275.2:n.158+28912_158+28922del
ENST00000613374.5:c.159-27945_159-27935del	ENSP00000484464.1:n.159-27945_159-27935del
ENST00000613706.5:c.906+468_906+478del	ENSP00000484976.2:n.906+468_906+478del
ENST00000617164.5:c.1257+60_1257+70del	ENSP00000480470.1:n.1257+60_1257+70del
ENST00000619009.5:c.364+11797_364+11807del	ENSP00000482293.1:n.364+11797_364+11807del
ENST00000650978.1:c.1156+60_1156+70del
ENST00000260947.8:c.1314+60_1314+70del	ENSP00000260947.4:n.1314+60_1314+70del
ENST00000421162.1:c.215+16561_215+16571del	ENSP00000392245.1:n.215+16561_215+16571del
ENST00000455743.5:c.*934+60_*934+70del	ENSP00000412186.1:n.*934+60_*934+70del
ENST00000613192.1:c.73+28912_73+28922del	ENSP00000483275.1:n.73+28912_73+28922del
ENST00000613374.4:c.159-27945_159-27935del	ENSP00000484464.1:n.159-27945_159-27935del
ENST00000613706.4:c.215+16561_215+16571del	ENSP00000484976.1:n.215+16561_215+16571del
ENST00000617164.4:c.1257+60_1257+70del	ENSP00000480470.1:n.1257+60_1257+70del
ENST00000619009.4:c.364+11797_364+11807del	ENSP00000482293.1:n.364+11797_364+11807del
ENST00000620057.4:c.365-11188_365-11178del	ENSP00000481988.1:n.365-11188_365-11178del
NM_000465.3:c.1314+60_1314+70del	NP_000456.2:n.1314+60_1314+70del
NM_001282543.1:c.1257+60_1257+70del	NP_001269472.1:n.1257+60_1257+70del
NM_001282545.1:c.215+16561_215+16571del	NP_001269474.1:n.215+16561_215+16571del
NM_001282548.1:c.159-27945_159-27935del	NP_001269477.1:n.159-27945_159-27935del
NM_001282549.1:c.364+11797_364+11807del	NP_001269478.1:n.364+11797_364+11807del
NR_104212.1:n.1307+60_1307+70del
NR_104215.1:n.1250+60_1250+70del
NR_104216.1:n.507-11188_507-11178del
XM_011511567.1:c.1260+60_1260+70del	XP_011509869.1:n.1260+60_1260+70del
XM_011511568.1:c.1314+60_1314+70del	XP_011509870.1:n.1314+60_1314+70del
XM_017004613.1:c.1413+60_1413+70del	XP_016860102.1:n.1413+60_1413+70del
XM_017004614.1:c.1413+60_1413+70del	XP_016860103.1:n.1413+60_1413+70del
XR_002959322.1:n.1504+60_1504+70del
NM_000465.4:c.1314+60_1314+70del MANE Select	NP_000456.2:n.1314+60_1314+70del
NM_001282543.2:c.1257+60_1257+70del	NP_001269472.1:n.1257+60_1257+70del
NM_001282545.2:c.215+16561_215+16571del	NP_001269474.1:n.215+16561_215+16571del
NM_001282548.2:c.159-27945_159-27935del	NP_001269477.1:n.159-27945_159-27935del
NM_001282549.2:c.364+11797_364+11807del	NP_001269478.1:n.364+11797_364+11807del
NR_104212.2:n.1279+60_1279+70del
NR_104215.2:n.1222+60_1222+70del
NR_104216.2:n.479-11188_479-11178del