Canonical Allele Identifier: CA658657221

Gene: BARD1

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214745719C>A , CM000664.2:g.214745719C>A	GRCh38
NC_000002.11:g.215610443C>A , CM000664.1:g.215610443C>A	GRCh37
NC_000002.10:g.215318688C>A	NCBI36
NG_012047.2:g.68986G>T
NG_012047.3:g.68993G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.1810+3G>T MANE Select	ENSP00000260947.4:n.1810+3G>T
ENST00000421162.2:c.457+3G>T	ENSP00000392245.2:n.457+3G>T
ENST00000613192.2:c.159-15211G>T	ENSP00000483275.2:n.159-15211G>T
ENST00000613374.5:c.400+3G>T	ENSP00000484464.1:n.400+3G>T
ENST00000613706.5:c.1402+3G>T	ENSP00000484976.2:n.1402+3G>T
ENST00000617164.5:c.1753+3G>T	ENSP00000480470.1:n.1753+3G>T
ENST00000619009.5:c.365-15211G>T	ENSP00000482293.1:n.365-15211G>T
ENST00000650978.1:c.3185+3G>T
ENST00000260947.8:c.1810+3G>T	ENSP00000260947.4:n.1810+3G>T
ENST00000421162.1:c.457+3G>T	ENSP00000392245.1:n.457+3G>T
ENST00000455743.5:c.*1430+3G>T	ENSP00000412186.1:n.*1430+3G>T
ENST00000465841.1:n.168G>T
ENST00000613192.1:c.74-15211G>T	ENSP00000483275.1:n.74-15211G>T
ENST00000613374.4:c.400+3G>T	ENSP00000484464.1:n.400+3G>T
ENST00000613706.4:c.457+3G>T	ENSP00000484976.1:n.457+3G>T
ENST00000617164.4:c.1753+3G>T	ENSP00000480470.1:n.1753+3G>T
ENST00000619009.4:c.365-15211G>T	ENSP00000482293.1:n.365-15211G>T
ENST00000620057.4:c.*476+3G>T	ENSP00000481988.1:n.*476+3G>T
NM_000465.3:c.1810+3G>T	NP_000456.2:n.1810+3G>T
NM_001282543.1:c.1753+3G>T	NP_001269472.1:n.1753+3G>T
NM_001282545.1:c.457+3G>T	NP_001269474.1:n.457+3G>T
NM_001282548.1:c.400+3G>T	NP_001269477.1:n.400+3G>T
NM_001282549.1:c.365-15211G>T	NP_001269478.1:n.365-15211G>T
NR_104212.1:n.1803+3G>T
NR_104215.1:n.1746+3G>T
NR_104216.1:n.1002+3G>T
XM_011511567.1:c.1756+3G>T	XP_011509869.1:n.1756+3G>T
XM_011511568.1:c.1810+3G>T	XP_011509870.1:n.1810+3G>T
XM_017004613.1:c.1909+3G>T	XP_016860102.1:n.1909+3G>T
XM_017004614.1:c.1909+3G>T	XP_016860103.1:n.1909+3G>T
XR_002959322.1:n.2000+3G>T
NM_000465.4:c.1810+3G>T MANE Select	NP_000456.2:n.1810+3G>T
NM_001282543.2:c.1753+3G>T	NP_001269472.1:n.1753+3G>T
NM_001282545.2:c.457+3G>T	NP_001269474.1:n.457+3G>T
NM_001282548.2:c.400+3G>T	NP_001269477.1:n.400+3G>T
NM_001282549.2:c.365-15211G>T	NP_001269478.1:n.365-15211G>T
NR_104212.2:n.1775+3G>T
NR_104215.2:n.1718+3G>T
NR_104216.2:n.974+3G>T