Canonical Allele Identifier: CA2527985761
Gene: BARD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214752414_214752415insATTTCAGACAC , CM000664.2:g.214752414_214752415insATTTCAGACAC GRCh38
NC_000002.11:g.215617138_215617139insATTTCAGACAC , CM000664.1:g.215617138_215617139insATTTCAGACAC GRCh37
NC_000002.10:g.215325383_215325384insATTTCAGACAC NCBI36
NG_012047.2:g.62290_62291insGTGTCTGAAAT
NG_012047.3:g.62297_62298insGTGTCTGAAAT

Transcript Alleles

HGVS Amino-acid change
ENST00000260947.9:c.1677+32_1677+33insGTGTCTGAAAT MANE Select ENSP00000260947.4:n.1677+32_1677+33insGTG...
ENST00000421162.2:c.324+32_324+33insGTGTCTGAAAT ENSP00000392245.2:n.324+32_324+33insGTGTC...
ENST00000613192.2:c.159-21907_159-21906insGTGTCTGAAAT ENSP00000483275.2:n.159-21907_159-21906in...
ENST00000613374.5:c.267+32_267+33insGTGTCTGAAAT ENSP00000484464.1:n.267+32_267+33insGTGTC...
ENST00000613706.5:c.1269+32_1269+33insGTGTCTGAAAT ENSP00000484976.2:n.1269+32_1269+33insGTG...
ENST00000617164.5:c.1620+32_1620+33insGTGTCTGAAAT ENSP00000480470.1:n.1620+32_1620+33insGTG...
ENST00000619009.5:c.365-21907_365-21906insGTGTCTGAAAT ENSP00000482293.1:n.365-21907_365-21906in...
ENST00000650978.1:c.3052+32_3052+33insGTGTCTGAAAT
ENST00000260947.8:c.1677+32_1677+33insGTGTCTGAAAT ENSP00000260947.4:n.1677+32_1677+33insGTG...
ENST00000421162.1:c.324+32_324+33insGTGTCTGAAAT ENSP00000392245.1:n.324+32_324+33insGTGTC...
ENST00000455743.5:c.*1297+32_*1297+33insGTGTCTGAAAT ENSP00000412186.1:n.*1297+32_*1297+33insG...
ENST00000465841.1:n.32+32_32+33insGTGTCTGAAAT
ENST00000613192.1:c.74-21907_74-21906insGTGTCTGAAAT ENSP00000483275.1:n.74-21907_74-21906insG...
ENST00000613374.4:c.267+32_267+33insGTGTCTGAAAT ENSP00000484464.1:n.267+32_267+33insGTGTC...
ENST00000613706.4:c.324+32_324+33insGTGTCTGAAAT ENSP00000484976.1:n.324+32_324+33insGTGTC...
ENST00000617164.4:c.1620+32_1620+33insGTGTCTGAAAT ENSP00000480470.1:n.1620+32_1620+33insGTG...
ENST00000619009.4:c.365-21907_365-21906insGTGTCTGAAAT ENSP00000482293.1:n.365-21907_365-21906in...
ENST00000620057.4:c.*343+32_*343+33insGTGTCTGAAAT ENSP00000481988.1:n.*343+32_*343+33insGTG...
NM_000465.3:c.1677+32_1677+33insGTGTCTGAAAT NP_000456.2:n.1677+32_1677+33insGTGTCTGAA...
NM_001282543.1:c.1620+32_1620+33insGTGTCTGAAAT NP_001269472.1:n.1620+32_1620+33insGTGTCT...
NM_001282545.1:c.324+32_324+33insGTGTCTGAAAT NP_001269474.1:n.324+32_324+33insGTGTCTGA...
NM_001282548.1:c.267+32_267+33insGTGTCTGAAAT NP_001269477.1:n.267+32_267+33insGTGTCTGA...
NM_001282549.1:c.365-21907_365-21906insGTGTCTGAAAT NP_001269478.1:n.365-21907_365-21906insGT...
NR_104212.1:n.1670+32_1670+33insGTGTCTGAAAT
NR_104215.1:n.1613+32_1613+33insGTGTCTGAAAT
NR_104216.1:n.869+32_869+33insGTGTCTGAAAT
XM_011511567.1:c.1623+32_1623+33insGTGTCTGAAAT XP_011509869.1:n.1623+32_1623+33insGTGTCT...
XM_011511568.1:c.1677+32_1677+33insGTGTCTGAAAT XP_011509870.1:n.1677+32_1677+33insGTGTCT...
XM_017004613.1:c.1776+32_1776+33insGTGTCTGAAAT XP_016860102.1:n.1776+32_1776+33insGTGTCT...
XM_017004614.1:c.1776+32_1776+33insGTGTCTGAAAT XP_016860103.1:n.1776+32_1776+33insGTGTCT...
XR_002959322.1:n.1867+32_1867+33insGTGTCTGAAAT
NM_000465.4:c.1677+32_1677+33insGTGTCTGAAAT MANE Select NP_000456.2:n.1677+32_1677+33insGTGTCTGAA...
NM_001282543.2:c.1620+32_1620+33insGTGTCTGAAAT NP_001269472.1:n.1620+32_1620+33insGTGTCT...
NM_001282545.2:c.324+32_324+33insGTGTCTGAAAT NP_001269474.1:n.324+32_324+33insGTGTCTGA...
NM_001282548.2:c.267+32_267+33insGTGTCTGAAAT NP_001269477.1:n.267+32_267+33insGTGTCTGA...
NM_001282549.2:c.365-21907_365-21906insGTGTCTGAAAT NP_001269478.1:n.365-21907_365-21906insGT...
NR_104212.2:n.1642+32_1642+33insGTGTCTGAAAT
NR_104215.2:n.1585+32_1585+33insGTGTCTGAAAT
NR_104216.2:n.841+32_841+33insGTGTCTGAAAT