Canonical Allele Identifier: CA350455498

Gene: BARD1

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214781059A>G , CM000664.2:g.214781059A>G	GRCh38
NC_000002.11:g.215645783A>G , CM000664.1:g.215645783A>G	GRCh37
NC_000002.10:g.215354028A>G	NCBI36
NG_012047.2:g.33646T>C
NG_012047.3:g.33653T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.815T>C MANE Select	ENSP00000260947.4:p.Phe272Ser
ENST00000421162.2:c.215+16002T>C	ENSP00000392245.2:n.215+16002T>C
ENST00000613192.2:c.158+28353T>C	ENSP00000483275.2:n.158+28353T>C
ENST00000613374.5:c.158+28353T>C	ENSP00000484464.1:n.158+28353T>C
ENST00000613706.5:c.815T>C	ENSP00000484976.2:p.Phe272Ser
ENST00000617164.5:c.758T>C	ENSP00000480470.1:p.Phe253Ser
ENST00000619009.5:c.364+11238T>C	ENSP00000482293.1:n.364+11238T>C
ENST00000650978.1:c.657T>C
ENST00000260947.8:c.815T>C	ENSP00000260947.4:p.Phe272Ser
ENST00000421162.1:c.215+16002T>C	ENSP00000392245.1:n.215+16002T>C
ENST00000455743.5:c.*435T>C	ENSP00000412186.1:n.*435T>C
ENST00000471787.1:n.710T>C
ENST00000613192.1:c.73+28353T>C	ENSP00000483275.1:n.73+28353T>C
ENST00000613374.4:c.158+28353T>C	ENSP00000484464.1:n.158+28353T>C
ENST00000613706.4:c.215+16002T>C	ENSP00000484976.1:n.215+16002T>C
ENST00000617164.4:c.758T>C	ENSP00000480470.1:p.Phe253Ser
ENST00000619009.4:c.364+11238T>C	ENSP00000482293.1:n.364+11238T>C
ENST00000620057.4:c.364+11238T>C	ENSP00000481988.1:n.364+11238T>C
NM_000465.3:c.815T>C	NP_000456.2:p.Phe272Ser
NM_001282543.1:c.758T>C	NP_001269472.1:p.Phe253Ser
NM_001282545.1:c.215+16002T>C	NP_001269474.1:n.215+16002T>C
NM_001282548.1:c.158+28353T>C	NP_001269477.1:n.158+28353T>C
NM_001282549.1:c.364+11238T>C	NP_001269478.1:n.364+11238T>C
NR_104212.1:n.808T>C
NR_104215.1:n.751T>C
NR_104216.1:n.506+11238T>C
XM_011511567.1:c.761T>C	XP_011509869.1:p.Phe254Ser
XM_011511568.1:c.815T>C	XP_011509870.1:p.Phe272Ser
XM_017004613.1:c.914T>C	XP_016860102.1:p.Phe305Ser
XM_017004614.1:c.914T>C	XP_016860103.1:p.Phe305Ser
XR_002959322.1:n.1005T>C
NM_000465.4:c.815T>C MANE Select	NP_000456.2:p.Phe272Ser
NM_001282543.2:c.758T>C	NP_001269472.1:p.Phe253Ser
NM_001282545.2:c.215+16002T>C	NP_001269474.1:n.215+16002T>C
NM_001282548.2:c.158+28353T>C	NP_001269477.1:n.158+28353T>C
NM_001282549.2:c.364+11238T>C	NP_001269478.1:n.364+11238T>C
NR_104212.2:n.780T>C
NR_104215.2:n.723T>C
NR_104216.2:n.478+11238T>C