Canonical Allele Identifier: CA1327057330

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214752428A= , CM000664.2:g.214752428A=	GRCh38
NC_000002.11:g.215617152A= , CM000664.1:g.215617152A=	GRCh37
NC_000002.10:g.215325397A=	NCBI36
NG_012047.2:g.62277T=
NG_012047.3:g.62284T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000260947.9:c.1677+19T= MANE Select	ENSP00000260947.4:n.1677+19T=
ENST00000421162.2:c.324+19T=	ENSP00000392245.2:n.324+19T=
ENST00000613192.2:c.159-21920T=	ENSP00000483275.2:n.159-21920T=
ENST00000613374.5:c.267+19T=	ENSP00000484464.1:n.267+19T=
ENST00000613706.5:c.1269+19T=	ENSP00000484976.2:n.1269+19T=
ENST00000617164.5:c.1620+19T=	ENSP00000480470.1:n.1620+19T=
ENST00000619009.5:c.365-21920T=	ENSP00000482293.1:n.365-21920T=
ENST00000650978.1:c.3052+19T=
ENST00000260947.8:c.1677+19T=	ENSP00000260947.4:n.1677+19T=
ENST00000421162.1:c.324+19T=	ENSP00000392245.1:n.324+19T=
ENST00000455743.5:c.*1297+19T=	ENSP00000412186.1:n.*1297+19T=
ENST00000465841.1:n.32+19T=
ENST00000613192.1:c.74-21920T=	ENSP00000483275.1:n.74-21920T=
ENST00000613374.4:c.267+19T=	ENSP00000484464.1:n.267+19T=
ENST00000613706.4:c.324+19T=	ENSP00000484976.1:n.324+19T=
ENST00000617164.4:c.1620+19T=	ENSP00000480470.1:n.1620+19T=
ENST00000619009.4:c.365-21920T=	ENSP00000482293.1:n.365-21920T=
ENST00000620057.4:c.*343+19T=	ENSP00000481988.1:n.*343+19T=
NM_000465.3:c.1677+19T=	NP_000456.2:n.1677+19T=
NM_001282543.1:c.1620+19T=	NP_001269472.1:n.1620+19T=
NM_001282545.1:c.324+19T=	NP_001269474.1:n.324+19T=
NM_001282548.1:c.267+19T=	NP_001269477.1:n.267+19T=
NM_001282549.1:c.365-21920T=	NP_001269478.1:n.365-21920T=
NR_104212.1:n.1670+19T=
NR_104215.1:n.1613+19T=
NR_104216.1:n.869+19T=
XM_011511567.1:c.1623+19T=	XP_011509869.1:n.1623+19T=
XM_011511568.1:c.1677+19T=	XP_011509870.1:n.1677+19T=
XM_017004613.1:c.1776+19T=	XP_016860102.1:n.1776+19T=
XM_017004614.1:c.1776+19T=	XP_016860103.1:n.1776+19T=
XR_002959322.1:n.1867+19T=
NM_000465.4:c.1677+19T= MANE Select	NP_000456.2:n.1677+19T=
NM_001282543.2:c.1620+19T=	NP_001269472.1:n.1620+19T=
NM_001282545.2:c.324+19T=	NP_001269474.1:n.324+19T=
NM_001282548.2:c.267+19T=	NP_001269477.1:n.267+19T=
NM_001282549.2:c.365-21920T=	NP_001269478.1:n.365-21920T=
NR_104212.2:n.1642+19T=
NR_104215.2:n.1585+19T=
NR_104216.2:n.841+19T=