Canonical Allele Identifier: CA1327085286
Gene: BARD1 HGNC NCBI

Linked Data

dbSNP Id: rs1574870397

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214809601G>A , CM000664.2:g.214809601G>A GRCh38
NC_000002.11:g.215674325G>A , CM000664.1:g.215674325G>A GRCh37
NC_000002.10:g.215382570G>A NCBI36
NG_012047.2:g.5104C>T
NG_012047.3:g.5111C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000260947.9:c.-32C>T MANE Select ENSP00000260947.4:n.-32C>T
ENST00000613192.2:c.-32C>T ENSP00000483275.2:n.-32C>T
ENST00000613374.5:c.-32C>T ENSP00000484464.1:n.-32C>T
ENST00000613706.5:c.-32C>T ENSP00000484976.2:n.-32C>T
ENST00000617164.5:c.-32C>T ENSP00000480470.1:n.-32C>T
ENST00000260947.8:c.-32C>T ENSP00000260947.4:n.-32C>T
ENST00000421162.1:c.-32C>T ENSP00000392245.1:n.-32C>T
ENST00000455743.5:c.-32C>T ENSP00000412186.1:n.-32C>T
ENST00000471787.1:n.70C>T
ENST00000479904.1:n.60C>T
ENST00000613192.1:c.-117C>T ENSP00000483275.1:n.-117C>T
ENST00000613374.4:c.-32C>T ENSP00000484464.1:n.-32C>T
ENST00000613706.4:c.-32C>T ENSP00000484976.1:n.-32C>T
ENST00000617164.4:c.-32C>T ENSP00000480470.1:n.-32C>T
ENST00000619009.4:c.-32C>T ENSP00000482293.1:n.-32C>T
ENST00000620057.4:c.-32C>T ENSP00000481988.1:n.-32C>T
NM_000465.3:c.-32C>T NP_000456.2:n.-32C>T
NM_001282543.1:c.-32C>T NP_001269472.1:n.-32C>T
NM_001282545.1:c.-32C>T NP_001269474.1:n.-32C>T
NM_001282548.1:c.-32C>T NP_001269477.1:n.-32C>T
NM_001282549.1:c.-32C>T NP_001269478.1:n.-32C>T
NR_104212.1:n.111C>T
NR_104215.1:n.111C>T
NR_104216.1:n.111C>T
XM_011511568.1:c.-32C>T XP_011509870.1:n.-32C>T
XM_017004613.1:c.-32C>T XP_016860102.1:n.-32C>T
XM_017004614.1:c.-32C>T XP_016860103.1:n.-32C>T
XR_002959322.1:n.60C>T
NM_000465.4:c.-32C>T MANE Select NP_000456.2:n.-32C>T
NM_001282543.2:c.-32C>T NP_001269472.1:n.-32C>T
NM_001282545.2:c.-32C>T NP_001269474.1:n.-32C>T
NM_001282548.2:c.-32C>T NP_001269477.1:n.-32C>T
NM_001282549.2:c.-32C>T NP_001269478.1:n.-32C>T
NR_104212.2:n.83C>T
NR_104215.2:n.83C>T
NR_104216.2:n.83C>T