Canonical Allele Identifier: CA2754203575
Gene: BARD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214745108_214745109insCACCCAA , CM000664.2:g.214745108_214745109insCACCCAA GRCh38
NC_000002.11:g.215609832_215609833insCACCCAA , CM000664.1:g.215609832_215609833insCACCCAA GRCh37
NC_000002.10:g.215318077_215318078insCACCCAA NCBI36
NG_012047.2:g.69597_69598insTGGGTGT
NG_012047.3:g.69604_69605insTGGGTGT

Transcript Alleles

HGVS Amino-acid change
ENST00000260947.9:c.1862_1863insTGGGTGT MANE Select ENSP00000260947.4:p.Met621IlefsTer16
ENST00000421162.2:c.509_510insTGGGTGT ENSP00000392245.2:p.Met170IlefsTer16
ENST00000613192.2:c.159-14600_159-14599insTGGGTGT ENSP00000483275.2:n.159-14600_159-14599in...
ENST00000613374.5:c.452_453insTGGGTGT ENSP00000484464.1:p.Met151IlefsTer16
ENST00000613706.5:c.1454_1455insTGGGTGT ENSP00000484976.2:p.Met485IlefsTer16
ENST00000617164.5:c.1805_1806insTGGGTGT ENSP00000480470.1:p.Met602IlefsTer16
ENST00000619009.5:c.365-14600_365-14599insTGGGTGT ENSP00000482293.1:n.365-14600_365-14599in...
ENST00000650978.1:c.3237_3238insTGGGTGT
ENST00000260947.8:c.1862_1863insTGGGTGT ENSP00000260947.4:p.Met621IlefsTer16
ENST00000421162.1:c.509_510insTGGGTGT ENSP00000392245.1:p.Met170IlefsTer16
ENST00000455743.5:c.*1482_*1483insTGGGTGT ENSP00000412186.1:n.*1482_*1483insTGGGTGT...
ENST00000613192.1:c.74-14600_74-14599insTGGGTGT ENSP00000483275.1:n.74-14600_74-14599insT...
ENST00000613374.4:c.452_453insTGGGTGT ENSP00000484464.1:p.Met151IlefsTer16
ENST00000613706.4:c.509_510insTGGGTGT ENSP00000484976.1:p.Met170IlefsTer16
ENST00000617164.4:c.1805_1806insTGGGTGT ENSP00000480470.1:p.Met602IlefsTer16
ENST00000619009.4:c.365-14600_365-14599insTGGGTGT ENSP00000482293.1:n.365-14600_365-14599in...
ENST00000620057.4:c.*528_*529insTGGGTGT ENSP00000481988.1:n.*528_*529insTGGGTGT
NM_000465.3:c.1862_1863insTGGGTGT NP_000456.2:p.Met621IlefsTer16
NM_001282543.1:c.1805_1806insTGGGTGT NP_001269472.1:p.Met602IlefsTer16
NM_001282545.1:c.509_510insTGGGTGT NP_001269474.1:p.Met170IlefsTer16
NM_001282548.1:c.452_453insTGGGTGT NP_001269477.1:p.Met151IlefsTer16
NM_001282549.1:c.365-14600_365-14599insTGGGTGT NP_001269478.1:n.365-14600_365-14599insTG...
NR_104212.1:n.1855_1856insTGGGTGT
NR_104215.1:n.1798_1799insTGGGTGT
NR_104216.1:n.1054_1055insTGGGTGT
XM_011511567.1:c.1808_1809insTGGGTGT XP_011509869.1:p.Met603IlefsTer16
XM_011511568.1:c.1862_1863insTGGGTGT XP_011509870.1:p.Met621IlefsTer16
XM_017004613.1:c.1961_1962insTGGGTGT XP_016860102.1:p.Met654IlefsTer16
XM_017004614.1:c.1961_1962insTGGGTGT XP_016860103.1:p.Met654IlefsTer16
XR_002959322.1:n.2052_2053insTGGGTGT
NM_000465.4:c.1862_1863insTGGGTGT MANE Select NP_000456.2:p.Met621IlefsTer16
NM_001282543.2:c.1805_1806insTGGGTGT NP_001269472.1:p.Met602IlefsTer16
NM_001282545.2:c.509_510insTGGGTGT NP_001269474.1:p.Met170IlefsTer16
NM_001282548.2:c.452_453insTGGGTGT NP_001269477.1:p.Met151IlefsTer16
NM_001282549.2:c.365-14600_365-14599insTGGGTGT NP_001269478.1:n.365-14600_365-14599insTG...
NR_104212.2:n.1827_1828insTGGGTGT
NR_104215.2:n.1770_1771insTGGGTGT
NR_104216.2:n.1026_1027insTGGGTGT