Canonical Allele Identifier: CA350453068
Community Standard Title: NM_000465.4(BARD1):c.1736C>A (p.Ser579Ter)
Gene: BARD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214745796G>T , CM000664.2:g.214745796G>T GRCh38
NC_000002.11:g.215610520G>T , CM000664.1:g.215610520G>T GRCh37
NC_000002.10:g.215318765G>T NCBI36
NG_012047.2:g.68909C>A
NG_012047.3:g.68916C>A

Transcript Alleles

HGVS Amino-acid Change
NM_000465.4:c.1736C>A MANE Select NP_000456.2:p.Ser579Ter
ENST00000260947.9:c.1736C>A MANE Select ENSP00000260947.4:p.Ser579Ter
NM_000465.3:c.1736C>A NP_000456.2:p.Ser579Ter
NM_001282543.1:c.1679C>A NP_001269472.1:p.Ser560Ter
NM_001282543.2:c.1679C>A NP_001269472.1:p.Ser560Ter
NM_001282545.1:c.383C>A NP_001269474.1:p.Ser128Ter
NM_001282545.2:c.383C>A NP_001269474.1:p.Ser128Ter
NM_001282548.1:c.326C>A NP_001269477.1:p.Ser109Ter
NM_001282548.2:c.326C>A NP_001269477.1:p.Ser109Ter
NM_001282549.1:c.365-15288C>A NP_001269478.1:n.365-15288C>A
NM_001282549.2:c.365-15288C>A NP_001269478.1:n.365-15288C>A
NR_104212.1:n.1729C>A
NR_104212.2:n.1701C>A
NR_104215.1:n.1672C>A
NR_104215.2:n.1644C>A
NR_104216.1:n.928C>A
NR_104216.2:n.900C>A
ENST00000260947.8:c.1736C>A ENSP00000260947.4:p.Ser579Ter
ENST00000421162.1:c.383C>A ENSP00000392245.1:p.Ser128Ter
ENST00000421162.2:c.383C>A ENSP00000392245.2:p.Ser128Ter
ENST00000455743.5:c.*1356C>A ENSP00000412186.1:n.*1356C>A
ENST00000465841.1:n.91C>A
ENST00000613192.1:c.74-15288C>A ENSP00000483275.1:n.74-15288C>A
ENST00000613192.2:c.159-15288C>A ENSP00000483275.2:n.159-15288C>A
ENST00000613374.4:c.326C>A ENSP00000484464.1:p.Ser109Ter
ENST00000613374.5:c.326C>A ENSP00000484464.1:p.Ser109Ter
ENST00000613706.4:c.383C>A ENSP00000484976.1:p.Ser128Ter
ENST00000613706.5:c.1328C>A ENSP00000484976.2:p.Ser443Ter
ENST00000617164.4:c.1679C>A ENSP00000480470.1:p.Ser560Ter
ENST00000617164.5:c.1679C>A ENSP00000480470.1:p.Ser560Ter
ENST00000619009.4:c.365-15288C>A ENSP00000482293.1:n.365-15288C>A
ENST00000619009.5:c.365-15288C>A ENSP00000482293.1:n.365-15288C>A
ENST00000620057.4:c.*402C>A ENSP00000481988.1:n.*402C>A
ENST00000650978.1:c.3111C>A
XM_011511567.1:c.1682C>A XP_011509869.1:p.Ser561Ter
XM_011511568.1:c.1736C>A XP_011509870.1:p.Ser579Ter
XM_017004613.1:c.1835C>A XP_016860102.1:p.Ser612Ter
XM_017004614.1:c.1835C>A XP_016860103.1:p.Ser612Ter
XR_002959322.1:n.1926C>A