Canonical Allele Identifier: CA350460898

Gene: BARD1

Linked Data

• MyVariant Identifiers: chr2:g.215657063A>T (hg19) ; chr2:g.214792339A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214792339A>T , CM000664.2:g.214792339A>T	GRCh38
NC_000002.11:g.215657063A>T , CM000664.1:g.215657063A>T	GRCh37
NC_000002.10:g.215365308A>T	NCBI36
NG_012047.2:g.22366T>A
NG_012047.3:g.22373T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.322T>A MANE Select	ENSP00000260947.4:p.Cys108Ser
ENST00000421162.2:c.215+4722T>A	ENSP00000392245.2:n.215+4722T>A
ENST00000613192.2:c.158+17073T>A	ENSP00000483275.2:n.158+17073T>A
ENST00000613374.5:c.158+17073T>A	ENSP00000484464.1:n.158+17073T>A
ENST00000613706.5:c.322T>A	ENSP00000484976.2:p.Cys108Ser
ENST00000617164.5:c.265T>A	ENSP00000480470.1:p.Cys89Ser
ENST00000619009.5:c.322T>A	ENSP00000482293.1:p.Cys108Ser
ENST00000650978.1:c.164T>A
ENST00000260947.8:c.322T>A	ENSP00000260947.4:p.Cys108Ser
ENST00000421162.1:c.215+4722T>A	ENSP00000392245.1:n.215+4722T>A
ENST00000455743.5:c.215+4722T>A	ENSP00000412186.1:n.215+4722T>A
ENST00000471787.1:n.260-10830T>A
ENST00000613192.1:c.73+17073T>A	ENSP00000483275.1:n.73+17073T>A
ENST00000613374.4:c.158+17073T>A	ENSP00000484464.1:n.158+17073T>A
ENST00000613706.4:c.215+4722T>A	ENSP00000484976.1:n.215+4722T>A
ENST00000617164.4:c.265T>A	ENSP00000480470.1:p.Cys89Ser
ENST00000619009.4:c.322T>A	ENSP00000482293.1:p.Cys108Ser
ENST00000620057.4:c.322T>A	ENSP00000481988.1:p.Cys108Ser
NM_000465.3:c.322T>A	NP_000456.2:p.Cys108Ser
NM_001282543.1:c.265T>A	NP_001269472.1:p.Cys89Ser
NM_001282545.1:c.215+4722T>A	NP_001269474.1:n.215+4722T>A
NM_001282548.1:c.158+17073T>A	NP_001269477.1:n.158+17073T>A
NM_001282549.1:c.322T>A	NP_001269478.1:p.Cys108Ser
NR_104212.1:n.357+4722T>A
NR_104215.1:n.301-10830T>A
NR_104216.1:n.464T>A
XM_011511567.1:c.268T>A	XP_011509869.1:p.Cys90Ser
XM_011511568.1:c.322T>A	XP_011509870.1:p.Cys108Ser
XM_017004613.1:c.421T>A	XP_016860102.1:p.Cys141Ser
XM_017004614.1:c.421T>A	XP_016860103.1:p.Cys141Ser
XR_002959322.1:n.512T>A
NM_000465.4:c.322T>A MANE Select	NP_000456.2:p.Cys108Ser
NM_001282543.2:c.265T>A	NP_001269472.1:p.Cys89Ser
NM_001282545.2:c.215+4722T>A	NP_001269474.1:n.215+4722T>A
NM_001282548.2:c.158+17073T>A	NP_001269477.1:n.158+17073T>A
NM_001282549.2:c.322T>A	NP_001269478.1:p.Cys108Ser
NR_104212.2:n.329+4722T>A
NR_104215.2:n.273-10830T>A
NR_104216.2:n.436T>A