Canonical Allele Identifier: CA350454809

Gene: BARD1

Linked Data

• MyVariant Identifiers: chr2:g.215617227A>T (hg19) ; chr2:g.214752503A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214752503A>T , CM000664.2:g.214752503A>T	GRCh38
NC_000002.11:g.215617227A>T , CM000664.1:g.215617227A>T	GRCh37
NC_000002.10:g.215325472A>T	NCBI36
NG_012047.2:g.62202T>A
NG_012047.3:g.62209T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.1621T>A MANE Select	ENSP00000260947.4:p.Ser541Thr
ENST00000421162.2:c.268T>A	ENSP00000392245.2:p.Ser90Thr
ENST00000613192.2:c.159-21995T>A	ENSP00000483275.2:n.159-21995T>A
ENST00000613374.5:c.211T>A	ENSP00000484464.1:p.Ser71Thr
ENST00000613706.5:c.1213T>A	ENSP00000484976.2:p.Ser405Thr
ENST00000617164.5:c.1564T>A	ENSP00000480470.1:p.Ser522Thr
ENST00000619009.5:c.365-21995T>A	ENSP00000482293.1:n.365-21995T>A
ENST00000650978.1:c.2996T>A
ENST00000260947.8:c.1621T>A	ENSP00000260947.4:p.Ser541Thr
ENST00000421162.1:c.268T>A	ENSP00000392245.1:p.Ser90Thr
ENST00000455743.5:c.*1241T>A	ENSP00000412186.1:n.*1241T>A
ENST00000613192.1:c.74-21995T>A	ENSP00000483275.1:n.74-21995T>A
ENST00000613374.4:c.211T>A	ENSP00000484464.1:p.Ser71Thr
ENST00000613706.4:c.268T>A	ENSP00000484976.1:p.Ser90Thr
ENST00000617164.4:c.1564T>A	ENSP00000480470.1:p.Ser522Thr
ENST00000619009.4:c.365-21995T>A	ENSP00000482293.1:n.365-21995T>A
ENST00000620057.4:c.*287T>A	ENSP00000481988.1:n.*287T>A
NM_000465.3:c.1621T>A	NP_000456.2:p.Ser541Thr
NM_001282543.1:c.1564T>A	NP_001269472.1:p.Ser522Thr
NM_001282545.1:c.268T>A	NP_001269474.1:p.Ser90Thr
NM_001282548.1:c.211T>A	NP_001269477.1:p.Ser71Thr
NM_001282549.1:c.365-21995T>A	NP_001269478.1:n.365-21995T>A
NR_104212.1:n.1614T>A
NR_104215.1:n.1557T>A
NR_104216.1:n.813T>A
XM_011511567.1:c.1567T>A	XP_011509869.1:p.Ser523Thr
XM_011511568.1:c.1621T>A	XP_011509870.1:p.Ser541Thr
XM_017004613.1:c.1720T>A	XP_016860102.1:p.Ser574Thr
XM_017004614.1:c.1720T>A	XP_016860103.1:p.Ser574Thr
XR_002959322.1:n.1811T>A
NM_000465.4:c.1621T>A MANE Select	NP_000456.2:p.Ser541Thr
NM_001282543.2:c.1564T>A	NP_001269472.1:p.Ser522Thr
NM_001282545.2:c.268T>A	NP_001269474.1:p.Ser90Thr
NM_001282548.2:c.211T>A	NP_001269477.1:p.Ser71Thr
NM_001282549.2:c.365-21995T>A	NP_001269478.1:n.365-21995T>A
NR_104212.2:n.1586T>A
NR_104215.2:n.1529T>A
NR_104216.2:n.785T>A