Canonical Allele Identifier: CA431392302
Gene: BARD1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.215645521C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214780797C>T , CM000664.2:g.214780797C>T GRCh38
NC_000002.11:g.215645521C>T , CM000664.1:g.215645521C>T GRCh37
NC_000002.10:g.215353766C>T NCBI36
NG_012047.2:g.33908G>A
NG_012047.3:g.33915G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000260947.9:c.1077G>A MANE Select ENSP00000260947.4:p.Leu359=
ENST00000421162.2:c.215+16264G>A ENSP00000392245.2:n.215+16264G>A
ENST00000613192.2:c.158+28615G>A ENSP00000483275.2:n.158+28615G>A
ENST00000613374.5:c.159-28242G>A ENSP00000484464.1:n.159-28242G>A
ENST00000613706.5:c.906+171G>A ENSP00000484976.2:n.906+171G>A
ENST00000617164.5:c.1020G>A ENSP00000480470.1:p.Leu340=
ENST00000619009.5:c.364+11500G>A ENSP00000482293.1:n.364+11500G>A
ENST00000650978.1:c.919G>A
ENST00000260947.8:c.1077G>A ENSP00000260947.4:p.Leu359=
ENST00000421162.1:c.215+16264G>A ENSP00000392245.1:n.215+16264G>A
ENST00000455743.5:c.*697G>A ENSP00000412186.1:n.*697G>A
ENST00000613192.1:c.73+28615G>A ENSP00000483275.1:n.73+28615G>A
ENST00000613374.4:c.159-28242G>A ENSP00000484464.1:n.159-28242G>A
ENST00000613706.4:c.215+16264G>A ENSP00000484976.1:n.215+16264G>A
ENST00000617164.4:c.1020G>A ENSP00000480470.1:p.Leu340=
ENST00000619009.4:c.364+11500G>A ENSP00000482293.1:n.364+11500G>A
ENST00000620057.4:c.365-11485G>A ENSP00000481988.1:n.365-11485G>A
NM_000465.3:c.1077G>A NP_000456.2:p.Leu359=
NM_001282543.1:c.1020G>A NP_001269472.1:p.Leu340=
NM_001282545.1:c.215+16264G>A NP_001269474.1:n.215+16264G>A
NM_001282548.1:c.159-28242G>A NP_001269477.1:n.159-28242G>A
NM_001282549.1:c.364+11500G>A NP_001269478.1:n.364+11500G>A
NR_104212.1:n.1070G>A
NR_104215.1:n.1013G>A
NR_104216.1:n.507-11485G>A
XM_011511567.1:c.1023G>A XP_011509869.1:p.Leu341=
XM_011511568.1:c.1077G>A XP_011509870.1:p.Leu359=
XM_017004613.1:c.1176G>A XP_016860102.1:p.Leu392=
XM_017004614.1:c.1176G>A XP_016860103.1:p.Leu392=
XR_002959322.1:n.1267G>A
NM_000465.4:c.1077G>A MANE Select NP_000456.2:p.Leu359=
NM_001282543.2:c.1020G>A NP_001269472.1:p.Leu340=
NM_001282545.2:c.215+16264G>A NP_001269474.1:n.215+16264G>A
NM_001282548.2:c.159-28242G>A NP_001269477.1:n.159-28242G>A
NM_001282549.2:c.364+11500G>A NP_001269478.1:n.364+11500G>A
NR_104212.2:n.1042G>A
NR_104215.2:n.985G>A
NR_104216.2:n.479-11485G>A