Canonical Allele Identifier: CA2090366

Gene: BARD1

Linked Data

• ClinVar Variation Id: 485315
• ClinVar RCV Id: RCV000562313 ; RCV003607324
• dbSNP Id: rs751581520
• ExAC: 2:215645689 G / A
• gnomAD v4: 2-214780965-G-A
• MyVariant Identifiers: chr2:g.215645689G>A (hg19) ; chr2:g.214780965G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214780965G>A , CM000664.2:g.214780965G>A	GRCh38
NC_000002.11:g.215645689G>A , CM000664.1:g.215645689G>A	GRCh37
NC_000002.10:g.215353934G>A	NCBI36
NG_012047.2:g.33740C>T
NG_012047.3:g.33747C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.909C>T MANE Select	ENSP00000260947.4:p.Val303=
ENST00000421162.2:c.215+16096C>T	ENSP00000392245.2:n.215+16096C>T
ENST00000613192.2:c.158+28447C>T	ENSP00000483275.2:n.158+28447C>T
ENST00000613374.5:c.159-28410C>T	ENSP00000484464.1:n.159-28410C>T
ENST00000613706.5:c.906+3C>T	ENSP00000484976.2:n.906+3C>T
ENST00000617164.5:c.852C>T	ENSP00000480470.1:p.Val284=
ENST00000619009.5:c.364+11332C>T	ENSP00000482293.1:n.364+11332C>T
ENST00000650978.1:c.751C>T
ENST00000260947.8:c.909C>T	ENSP00000260947.4:p.Val303=
ENST00000421162.1:c.215+16096C>T	ENSP00000392245.1:n.215+16096C>T
ENST00000455743.5:c.*529C>T	ENSP00000412186.1:n.*529C>T
ENST00000471787.1:n.804C>T
ENST00000613192.1:c.73+28447C>T	ENSP00000483275.1:n.73+28447C>T
ENST00000613374.4:c.159-28410C>T	ENSP00000484464.1:n.159-28410C>T
ENST00000613706.4:c.215+16096C>T	ENSP00000484976.1:n.215+16096C>T
ENST00000617164.4:c.852C>T	ENSP00000480470.1:p.Val284=
ENST00000619009.4:c.364+11332C>T	ENSP00000482293.1:n.364+11332C>T
ENST00000620057.4:c.364+11332C>T	ENSP00000481988.1:n.364+11332C>T
NM_000465.3:c.909C>T	NP_000456.2:p.Val303=
NM_001282543.1:c.852C>T	NP_001269472.1:p.Val284=
NM_001282545.1:c.215+16096C>T	NP_001269474.1:n.215+16096C>T
NM_001282548.1:c.159-28410C>T	NP_001269477.1:n.159-28410C>T
NM_001282549.1:c.364+11332C>T	NP_001269478.1:n.364+11332C>T
NR_104212.1:n.902C>T
NR_104215.1:n.845C>T
NR_104216.1:n.506+11332C>T
XM_011511567.1:c.855C>T	XP_011509869.1:p.Val285=
XM_011511568.1:c.909C>T	XP_011509870.1:p.Val303=
XM_017004613.1:c.1008C>T	XP_016860102.1:p.Val336=
XM_017004614.1:c.1008C>T	XP_016860103.1:p.Val336=
XR_002959322.1:n.1099C>T
NM_000465.4:c.909C>T MANE Select	NP_000456.2:p.Val303=
NM_001282543.2:c.852C>T	NP_001269472.1:p.Val284=
NM_001282545.2:c.215+16096C>T	NP_001269474.1:n.215+16096C>T
NM_001282548.2:c.159-28410C>T	NP_001269477.1:n.159-28410C>T
NM_001282549.2:c.364+11332C>T	NP_001269478.1:n.364+11332C>T
NR_104212.2:n.874C>T
NR_104215.2:n.817C>T
NR_104216.2:n.478+11332C>T