Canonical Allele Identifier: CA2662970699

Gene: BARD1

Linked Data

• gnomAD v4: 2-214752391-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214752391T>C , CM000664.2:g.214752391T>C	GRCh38
NC_000002.11:g.215617115T>C , CM000664.1:g.215617115T>C	GRCh37
NC_000002.10:g.215325360T>C	NCBI36
NG_012047.2:g.62314A>G
NG_012047.3:g.62321A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000260947.9:c.1677+56A>G MANE Select	ENSP00000260947.4:n.1677+56A>G
ENST00000421162.2:c.324+56A>G	ENSP00000392245.2:n.324+56A>G
ENST00000613192.2:c.159-21883A>G	ENSP00000483275.2:n.159-21883A>G
ENST00000613374.5:c.267+56A>G	ENSP00000484464.1:n.267+56A>G
ENST00000613706.5:c.1269+56A>G	ENSP00000484976.2:n.1269+56A>G
ENST00000617164.5:c.1620+56A>G	ENSP00000480470.1:n.1620+56A>G
ENST00000619009.5:c.365-21883A>G	ENSP00000482293.1:n.365-21883A>G
ENST00000650978.1:c.3052+56A>G
ENST00000260947.8:c.1677+56A>G	ENSP00000260947.4:n.1677+56A>G
ENST00000421162.1:c.324+56A>G	ENSP00000392245.1:n.324+56A>G
ENST00000455743.5:c.*1297+56A>G	ENSP00000412186.1:n.*1297+56A>G
ENST00000465841.1:n.32+56A>G
ENST00000613192.1:c.74-21883A>G	ENSP00000483275.1:n.74-21883A>G
ENST00000613374.4:c.267+56A>G	ENSP00000484464.1:n.267+56A>G
ENST00000613706.4:c.324+56A>G	ENSP00000484976.1:n.324+56A>G
ENST00000617164.4:c.1620+56A>G	ENSP00000480470.1:n.1620+56A>G
ENST00000619009.4:c.365-21883A>G	ENSP00000482293.1:n.365-21883A>G
ENST00000620057.4:c.*343+56A>G	ENSP00000481988.1:n.*343+56A>G
NM_000465.3:c.1677+56A>G	NP_000456.2:n.1677+56A>G
NM_001282543.1:c.1620+56A>G	NP_001269472.1:n.1620+56A>G
NM_001282545.1:c.324+56A>G	NP_001269474.1:n.324+56A>G
NM_001282548.1:c.267+56A>G	NP_001269477.1:n.267+56A>G
NM_001282549.1:c.365-21883A>G	NP_001269478.1:n.365-21883A>G
NR_104212.1:n.1670+56A>G
NR_104215.1:n.1613+56A>G
NR_104216.1:n.869+56A>G
XM_011511567.1:c.1623+56A>G	XP_011509869.1:n.1623+56A>G
XM_011511568.1:c.1677+56A>G	XP_011509870.1:n.1677+56A>G
XM_017004613.1:c.1776+56A>G	XP_016860102.1:n.1776+56A>G
XM_017004614.1:c.1776+56A>G	XP_016860103.1:n.1776+56A>G
XR_002959322.1:n.1867+56A>G
NM_000465.4:c.1677+56A>G MANE Select	NP_000456.2:n.1677+56A>G
NM_001282543.2:c.1620+56A>G	NP_001269472.1:n.1620+56A>G
NM_001282545.2:c.324+56A>G	NP_001269474.1:n.324+56A>G
NM_001282548.2:c.267+56A>G	NP_001269477.1:n.267+56A>G
NM_001282549.2:c.365-21883A>G	NP_001269478.1:n.365-21883A>G
NR_104212.2:n.1642+56A>G
NR_104215.2:n.1585+56A>G
NR_104216.2:n.841+56A>G