Canonical Allele Identifier: CA431136582

Gene: BARD1

Linked Data

• MyVariant Identifiers: chr2:g.215646190T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214781466T>G , CM000664.2:g.214781466T>G	GRCh38
NC_000002.11:g.215646190T>G , CM000664.1:g.215646190T>G	GRCh37
NC_000002.10:g.215354435T>G	NCBI36
NG_012047.2:g.33239A>C
NG_012047.3:g.33246A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.408A>C MANE Select	ENSP00000260947.4:p.Ala136=
ENST00000421162.2:c.215+15595A>C	ENSP00000392245.2:n.215+15595A>C
ENST00000613192.2:c.158+27946A>C	ENSP00000483275.2:n.158+27946A>C
ENST00000613374.5:c.158+27946A>C	ENSP00000484464.1:n.158+27946A>C
ENST00000613706.5:c.408A>C	ENSP00000484976.2:p.Ala136=
ENST00000617164.5:c.351A>C	ENSP00000480470.1:p.Ala117=
ENST00000619009.5:c.364+10831A>C	ENSP00000482293.1:n.364+10831A>C
ENST00000650978.1:c.250A>C
ENST00000260947.8:c.408A>C	ENSP00000260947.4:p.Ala136=
ENST00000421162.1:c.215+15595A>C	ENSP00000392245.1:n.215+15595A>C
ENST00000455743.5:c.*28A>C	ENSP00000412186.1:n.*28A>C
ENST00000471787.1:n.303A>C
ENST00000613192.1:c.73+27946A>C	ENSP00000483275.1:n.73+27946A>C
ENST00000613374.4:c.158+27946A>C	ENSP00000484464.1:n.158+27946A>C
ENST00000613706.4:c.215+15595A>C	ENSP00000484976.1:n.215+15595A>C
ENST00000617164.4:c.351A>C	ENSP00000480470.1:p.Ala117=
ENST00000619009.4:c.364+10831A>C	ENSP00000482293.1:n.364+10831A>C
ENST00000620057.4:c.364+10831A>C	ENSP00000481988.1:n.364+10831A>C
NM_000465.3:c.408A>C	NP_000456.2:p.Ala136=
NM_001282543.1:c.351A>C	NP_001269472.1:p.Ala117=
NM_001282545.1:c.215+15595A>C	NP_001269474.1:n.215+15595A>C
NM_001282548.1:c.158+27946A>C	NP_001269477.1:n.158+27946A>C
NM_001282549.1:c.364+10831A>C	NP_001269478.1:n.364+10831A>C
NR_104212.1:n.401A>C
NR_104215.1:n.344A>C
NR_104216.1:n.506+10831A>C
XM_011511567.1:c.354A>C	XP_011509869.1:p.Ala118=
XM_011511568.1:c.408A>C	XP_011509870.1:p.Ala136=
XM_017004613.1:c.507A>C	XP_016860102.1:p.Ala169=
XM_017004614.1:c.507A>C	XP_016860103.1:p.Ala169=
XR_002959322.1:n.598A>C
NM_000465.4:c.408A>C MANE Select	NP_000456.2:p.Ala136=
NM_001282543.2:c.351A>C	NP_001269472.1:p.Ala117=
NM_001282545.2:c.215+15595A>C	NP_001269474.1:n.215+15595A>C
NM_001282548.2:c.158+27946A>C	NP_001269477.1:n.158+27946A>C
NM_001282549.2:c.364+10831A>C	NP_001269478.1:n.364+10831A>C
NR_104212.2:n.373A>C
NR_104215.2:n.316A>C
NR_104216.2:n.478+10831A>C