Canonical Allele Identifier: CA764591216

Gene: BARD1

Linked Data

• dbSNP Id: rs1370934873
• gnomAD v3: 2-214780443-T-A
• gnomAD v4: 2-214780443-T-A
• MyVariant Identifiers: chr2:g.215645167T>A (hg19) ; chr2:g.214780443T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214780443T>A , CM000664.2:g.214780443T>A	GRCh38
NC_000002.11:g.215645167T>A , CM000664.1:g.215645167T>A	GRCh37
NC_000002.10:g.215353412T>A	NCBI36
NG_012047.2:g.34262A>T
NG_012047.3:g.34269A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.1314+117A>T MANE Select	ENSP00000260947.4:n.1314+117A>T
ENST00000421162.2:c.215+16618A>T	ENSP00000392245.2:n.215+16618A>T
ENST00000613192.2:c.158+28969A>T	ENSP00000483275.2:n.158+28969A>T
ENST00000613374.5:c.159-27888A>T	ENSP00000484464.1:n.159-27888A>T
ENST00000613706.5:c.906+525A>T	ENSP00000484976.2:n.906+525A>T
ENST00000617164.5:c.1257+117A>T	ENSP00000480470.1:n.1257+117A>T
ENST00000619009.5:c.364+11854A>T	ENSP00000482293.1:n.364+11854A>T
ENST00000650978.1:c.1156+117A>T
ENST00000260947.8:c.1314+117A>T	ENSP00000260947.4:n.1314+117A>T
ENST00000421162.1:c.215+16618A>T	ENSP00000392245.1:n.215+16618A>T
ENST00000455743.5:c.*934+117A>T	ENSP00000412186.1:n.*934+117A>T
ENST00000613192.1:c.73+28969A>T	ENSP00000483275.1:n.73+28969A>T
ENST00000613374.4:c.159-27888A>T	ENSP00000484464.1:n.159-27888A>T
ENST00000613706.4:c.215+16618A>T	ENSP00000484976.1:n.215+16618A>T
ENST00000617164.4:c.1257+117A>T	ENSP00000480470.1:n.1257+117A>T
ENST00000619009.4:c.364+11854A>T	ENSP00000482293.1:n.364+11854A>T
ENST00000620057.4:c.365-11131A>T	ENSP00000481988.1:n.365-11131A>T
NM_000465.3:c.1314+117A>T	NP_000456.2:n.1314+117A>T
NM_001282543.1:c.1257+117A>T	NP_001269472.1:n.1257+117A>T
NM_001282545.1:c.215+16618A>T	NP_001269474.1:n.215+16618A>T
NM_001282548.1:c.159-27888A>T	NP_001269477.1:n.159-27888A>T
NM_001282549.1:c.364+11854A>T	NP_001269478.1:n.364+11854A>T
NR_104212.1:n.1307+117A>T
NR_104215.1:n.1250+117A>T
NR_104216.1:n.507-11131A>T
XM_011511567.1:c.1260+117A>T	XP_011509869.1:n.1260+117A>T
XM_011511568.1:c.1314+117A>T	XP_011509870.1:n.1314+117A>T
XM_017004613.1:c.1413+117A>T	XP_016860102.1:n.1413+117A>T
XM_017004614.1:c.1413+117A>T	XP_016860103.1:n.1413+117A>T
XR_002959322.1:n.1504+117A>T
NM_000465.4:c.1314+117A>T MANE Select	NP_000456.2:n.1314+117A>T
NM_001282543.2:c.1257+117A>T	NP_001269472.1:n.1257+117A>T
NM_001282545.2:c.215+16618A>T	NP_001269474.1:n.215+16618A>T
NM_001282548.2:c.159-27888A>T	NP_001269477.1:n.159-27888A>T
NM_001282549.2:c.364+11854A>T	NP_001269478.1:n.364+11854A>T
NR_104212.2:n.1279+117A>T
NR_104215.2:n.1222+117A>T
NR_104216.2:n.479-11131A>T