Canonical Allele Identifier: CA64788116

Gene: BARD1

Linked Data

• ClinVar Variation Id: 460689
• ClinVar RCV Id: RCV000532171 ; RCV002225649 ; RCV004023835
• dbSNP Id: rs568305044
• gnomAD v4: 2-214780756-C-T
• MyVariant Identifiers: chr2:g.215645480C>T (hg19) ; chr2:g.214780756C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214780756C>T , CM000664.2:g.214780756C>T	GRCh38
NC_000002.11:g.215645480C>T , CM000664.1:g.215645480C>T	GRCh37
NC_000002.10:g.215353725C>T	NCBI36
NG_012047.2:g.33949G>A
NG_012047.3:g.33956G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.1118G>A MANE Select	ENSP00000260947.4:p.Gly373Asp
ENST00000421162.2:c.215+16305G>A	ENSP00000392245.2:n.215+16305G>A
ENST00000613192.2:c.158+28656G>A	ENSP00000483275.2:n.158+28656G>A
ENST00000613374.5:c.159-28201G>A	ENSP00000484464.1:n.159-28201G>A
ENST00000613706.5:c.906+212G>A	ENSP00000484976.2:n.906+212G>A
ENST00000617164.5:c.1061G>A	ENSP00000480470.1:p.Gly354Asp
ENST00000619009.5:c.364+11541G>A	ENSP00000482293.1:n.364+11541G>A
ENST00000650978.1:c.960G>A
ENST00000260947.8:c.1118G>A	ENSP00000260947.4:p.Gly373Asp
ENST00000421162.1:c.215+16305G>A	ENSP00000392245.1:n.215+16305G>A
ENST00000455743.5:c.*738G>A	ENSP00000412186.1:n.*738G>A
ENST00000613192.1:c.73+28656G>A	ENSP00000483275.1:n.73+28656G>A
ENST00000613374.4:c.159-28201G>A	ENSP00000484464.1:n.159-28201G>A
ENST00000613706.4:c.215+16305G>A	ENSP00000484976.1:n.215+16305G>A
ENST00000617164.4:c.1061G>A	ENSP00000480470.1:p.Gly354Asp
ENST00000619009.4:c.364+11541G>A	ENSP00000482293.1:n.364+11541G>A
ENST00000620057.4:c.365-11444G>A	ENSP00000481988.1:n.365-11444G>A
NM_000465.3:c.1118G>A	NP_000456.2:p.Gly373Asp
NM_001282543.1:c.1061G>A	NP_001269472.1:p.Gly354Asp
NM_001282545.1:c.215+16305G>A	NP_001269474.1:n.215+16305G>A
NM_001282548.1:c.159-28201G>A	NP_001269477.1:n.159-28201G>A
NM_001282549.1:c.364+11541G>A	NP_001269478.1:n.364+11541G>A
NR_104212.1:n.1111G>A
NR_104215.1:n.1054G>A
NR_104216.1:n.507-11444G>A
XM_011511567.1:c.1064G>A	XP_011509869.1:p.Gly355Asp
XM_011511568.1:c.1118G>A	XP_011509870.1:p.Gly373Asp
XM_017004613.1:c.1217G>A	XP_016860102.1:p.Gly406Asp
XM_017004614.1:c.1217G>A	XP_016860103.1:p.Gly406Asp
XR_002959322.1:n.1308G>A
NM_000465.4:c.1118G>A MANE Select	NP_000456.2:p.Gly373Asp
NM_001282543.2:c.1061G>A	NP_001269472.1:p.Gly354Asp
NM_001282545.2:c.215+16305G>A	NP_001269474.1:n.215+16305G>A
NM_001282548.2:c.159-28201G>A	NP_001269477.1:n.159-28201G>A
NM_001282549.2:c.364+11541G>A	NP_001269478.1:n.364+11541G>A
NR_104212.2:n.1083G>A
NR_104215.2:n.1026G>A
NR_104216.2:n.479-11444G>A