Canonical Allele Identifier: CA193360

Gene: BARD1

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214780813G>C , CM000664.2:g.214780813G>C	GRCh38
NC_000002.11:g.215645537G>C , CM000664.1:g.215645537G>C	GRCh37
NC_000002.10:g.215353782G>C	NCBI36
NG_012047.2:g.33892C>G
NG_012047.3:g.33899C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.1061C>G MANE Select	ENSP00000260947.4:p.Ser354Ter
ENST00000421162.2:c.215+16248C>G	ENSP00000392245.2:n.215+16248C>G
ENST00000613192.2:c.158+28599C>G	ENSP00000483275.2:n.158+28599C>G
ENST00000613374.5:c.159-28258C>G	ENSP00000484464.1:n.159-28258C>G
ENST00000613706.5:c.906+155C>G	ENSP00000484976.2:n.906+155C>G
ENST00000617164.5:c.1004C>G	ENSP00000480470.1:p.Ser335Ter
ENST00000619009.5:c.364+11484C>G	ENSP00000482293.1:n.364+11484C>G
ENST00000650978.1:c.903C>G
ENST00000260947.8:c.1061C>G	ENSP00000260947.4:p.Ser354Ter
ENST00000421162.1:c.215+16248C>G	ENSP00000392245.1:n.215+16248C>G
ENST00000455743.5:c.*681C>G	ENSP00000412186.1:n.*681C>G
ENST00000613192.1:c.73+28599C>G	ENSP00000483275.1:n.73+28599C>G
ENST00000613374.4:c.159-28258C>G	ENSP00000484464.1:n.159-28258C>G
ENST00000613706.4:c.215+16248C>G	ENSP00000484976.1:n.215+16248C>G
ENST00000617164.4:c.1004C>G	ENSP00000480470.1:p.Ser335Ter
ENST00000619009.4:c.364+11484C>G	ENSP00000482293.1:n.364+11484C>G
ENST00000620057.4:c.364+11484C>G	ENSP00000481988.1:n.364+11484C>G
NM_000465.3:c.1061C>G	NP_000456.2:p.Ser354Ter
NM_001282543.1:c.1004C>G	NP_001269472.1:p.Ser335Ter
NM_001282545.1:c.215+16248C>G	NP_001269474.1:n.215+16248C>G
NM_001282548.1:c.159-28258C>G	NP_001269477.1:n.159-28258C>G
NM_001282549.1:c.364+11484C>G	NP_001269478.1:n.364+11484C>G
NR_104212.1:n.1054C>G
NR_104215.1:n.997C>G
NR_104216.1:n.506+11484C>G
XM_011511567.1:c.1007C>G	XP_011509869.1:p.Ser336Ter
XM_011511568.1:c.1061C>G	XP_011509870.1:p.Ser354Ter
XM_017004613.1:c.1160C>G	XP_016860102.1:p.Ser387Ter
XM_017004614.1:c.1160C>G	XP_016860103.1:p.Ser387Ter
XR_002959322.1:n.1251C>G
NM_000465.4:c.1061C>G MANE Select	NP_000456.2:p.Ser354Ter
NM_001282543.2:c.1004C>G	NP_001269472.1:p.Ser335Ter
NM_001282545.2:c.215+16248C>G	NP_001269474.1:n.215+16248C>G
NM_001282548.2:c.159-28258C>G	NP_001269477.1:n.159-28258C>G
NM_001282549.2:c.364+11484C>G	NP_001269478.1:n.364+11484C>G
NR_104212.2:n.1026C>G
NR_104215.2:n.969C>G
NR_104216.2:n.478+11484C>G