Canonical Allele Identifier: CA2662973039

Gene: BARD1

Linked Data

• gnomAD v4: 2-214809679-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214809679C>G , CM000664.2:g.214809679C>G	GRCh38
NC_000002.11:g.215674403C>G , CM000664.1:g.215674403C>G	GRCh37
NC_000002.10:g.215382648C>G	NCBI36
NG_012047.2:g.5026G>C
NG_012047.3:g.5033G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.-110G>C MANE Select	ENSP00000260947.4:n.-110G>C
ENST00000613192.2:c.-110G>C	ENSP00000483275.2:n.-110G>C
ENST00000613706.5:c.-110G>C	ENSP00000484976.2:n.-110G>C
ENST00000260947.8:c.-110G>C	ENSP00000260947.4:n.-110G>C
ENST00000421162.1:c.-110G>C	ENSP00000392245.1:n.-110G>C
ENST00000613192.1:c.-195G>C	ENSP00000483275.1:n.-195G>C
ENST00000613374.4:c.-110G>C	ENSP00000484464.1:n.-110G>C
ENST00000613706.4:c.-110G>C	ENSP00000484976.1:n.-110G>C
ENST00000617164.4:c.-110G>C	ENSP00000480470.1:n.-110G>C
ENST00000619009.4:c.-110G>C	ENSP00000482293.1:n.-110G>C
NM_000465.3:c.-110G>C	NP_000456.2:n.-110G>C
NM_001282543.1:c.-110G>C	NP_001269472.1:n.-110G>C
NM_001282545.1:c.-110G>C	NP_001269474.1:n.-110G>C
NM_001282548.1:c.-110G>C	NP_001269477.1:n.-110G>C
NM_001282549.1:c.-110G>C	NP_001269478.1:n.-110G>C
NR_104212.1:n.33G>C
NR_104215.1:n.33G>C
NR_104216.1:n.33G>C
XM_011511568.1:c.-110G>C	XP_011509870.1:n.-110G>C
NM_000465.4:c.-110G>C MANE Select	NP_000456.2:n.-110G>C
NM_001282543.2:c.-110G>C	NP_001269472.1:n.-110G>C
NM_001282545.2:c.-110G>C	NP_001269474.1:n.-110G>C
NM_001282548.2:c.-110G>C	NP_001269477.1:n.-110G>C
NM_001282549.2:c.-110G>C	NP_001269478.1:n.-110G>C
NR_104212.2:n.5G>C
NR_104215.2:n.5G>C
NR_104216.2:n.5G>C