Canonical Allele Identifier: CA350454142

Gene: BARD1

Linked Data

• ClinVar Variation Id: 479143
• ClinVar RCV Id: RCV000562704 ; RCV000690479
• dbSNP Id: rs1553622277
• MyVariant Identifiers: chr2:g.215645541G>A (hg19) ; chr2:g.214780817G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214780817G>A , CM000664.2:g.214780817G>A	GRCh38
NC_000002.11:g.215645541G>A , CM000664.1:g.215645541G>A	GRCh37
NC_000002.10:g.215353786G>A	NCBI36
NG_012047.2:g.33888C>T
NG_012047.3:g.33895C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000260947.9:c.1057C>T MANE Select	ENSP00000260947.4:p.Pro353Ser
ENST00000421162.2:c.215+16244C>T	ENSP00000392245.2:n.215+16244C>T
ENST00000613192.2:c.158+28595C>T	ENSP00000483275.2:n.158+28595C>T
ENST00000613374.5:c.159-28262C>T	ENSP00000484464.1:n.159-28262C>T
ENST00000613706.5:c.906+151C>T	ENSP00000484976.2:n.906+151C>T
ENST00000617164.5:c.1000C>T	ENSP00000480470.1:p.Pro334Ser
ENST00000619009.5:c.364+11480C>T	ENSP00000482293.1:n.364+11480C>T
ENST00000650978.1:c.899C>T
ENST00000260947.8:c.1057C>T	ENSP00000260947.4:p.Pro353Ser
ENST00000421162.1:c.215+16244C>T	ENSP00000392245.1:n.215+16244C>T
ENST00000455743.5:c.*677C>T	ENSP00000412186.1:n.*677C>T
ENST00000613192.1:c.73+28595C>T	ENSP00000483275.1:n.73+28595C>T
ENST00000613374.4:c.159-28262C>T	ENSP00000484464.1:n.159-28262C>T
ENST00000613706.4:c.215+16244C>T	ENSP00000484976.1:n.215+16244C>T
ENST00000617164.4:c.1000C>T	ENSP00000480470.1:p.Pro334Ser
ENST00000619009.4:c.364+11480C>T	ENSP00000482293.1:n.364+11480C>T
ENST00000620057.4:c.364+11480C>T	ENSP00000481988.1:n.364+11480C>T
NM_000465.3:c.1057C>T	NP_000456.2:p.Pro353Ser
NM_001282543.1:c.1000C>T	NP_001269472.1:p.Pro334Ser
NM_001282545.1:c.215+16244C>T	NP_001269474.1:n.215+16244C>T
NM_001282548.1:c.159-28262C>T	NP_001269477.1:n.159-28262C>T
NM_001282549.1:c.364+11480C>T	NP_001269478.1:n.364+11480C>T
NR_104212.1:n.1050C>T
NR_104215.1:n.993C>T
NR_104216.1:n.506+11480C>T
XM_011511567.1:c.1003C>T	XP_011509869.1:p.Pro335Ser
XM_011511568.1:c.1057C>T	XP_011509870.1:p.Pro353Ser
XM_017004613.1:c.1156C>T	XP_016860102.1:p.Pro386Ser
XM_017004614.1:c.1156C>T	XP_016860103.1:p.Pro386Ser
XR_002959322.1:n.1247C>T
NM_000465.4:c.1057C>T MANE Select	NP_000456.2:p.Pro353Ser
NM_001282543.2:c.1000C>T	NP_001269472.1:p.Pro334Ser
NM_001282545.2:c.215+16244C>T	NP_001269474.1:n.215+16244C>T
NM_001282548.2:c.159-28262C>T	NP_001269477.1:n.159-28262C>T
NM_001282549.2:c.364+11480C>T	NP_001269478.1:n.364+11480C>T
NR_104212.2:n.1022C>T
NR_104215.2:n.965C>T
NR_104216.2:n.478+11480C>T