Canonical Allele Identifier: CA2662970660

Gene: BARD1

Linked Data

• gnomAD v4: 2-214752341-TTGG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214752344_214752346del , CM000664.2:g.214752344_214752346del	GRCh38
NC_000002.11:g.215617068_215617070del , CM000664.1:g.215617068_215617070del	GRCh37
NC_000002.10:g.215325313_215325315del	NCBI36
NG_012047.2:g.62361_62363del
NG_012047.3:g.62368_62370del

Transcript Alleles

HGVS	Amino-acid change
ENST00000260947.9:c.1677+103_1677+105del MANE Select	ENSP00000260947.4:n.1677+103_1677+105del
ENST00000421162.2:c.324+103_324+105del	ENSP00000392245.2:n.324+103_324+105del
ENST00000613192.2:c.159-21836_159-21834del	ENSP00000483275.2:n.159-21836_159-21834de...
ENST00000613374.5:c.267+103_267+105del	ENSP00000484464.1:n.267+103_267+105del
ENST00000613706.5:c.1269+103_1269+105del	ENSP00000484976.2:n.1269+103_1269+105del
ENST00000617164.5:c.1620+103_1620+105del	ENSP00000480470.1:n.1620+103_1620+105del
ENST00000619009.5:c.365-21836_365-21834del	ENSP00000482293.1:n.365-21836_365-21834de...
ENST00000650978.1:c.3052+103_3052+105del
ENST00000260947.8:c.1677+103_1677+105del	ENSP00000260947.4:n.1677+103_1677+105del
ENST00000421162.1:c.324+103_324+105del	ENSP00000392245.1:n.324+103_324+105del
ENST00000455743.5:c.*1297+103_*1297+105del	ENSP00000412186.1:n.*1297+103_*1297+105de...
ENST00000465841.1:n.32+103_32+105del
ENST00000613192.1:c.74-21836_74-21834del	ENSP00000483275.1:n.74-21836_74-21834del
ENST00000613374.4:c.267+103_267+105del	ENSP00000484464.1:n.267+103_267+105del
ENST00000613706.4:c.324+103_324+105del	ENSP00000484976.1:n.324+103_324+105del
ENST00000617164.4:c.1620+103_1620+105del	ENSP00000480470.1:n.1620+103_1620+105del
ENST00000619009.4:c.365-21836_365-21834del	ENSP00000482293.1:n.365-21836_365-21834de...
ENST00000620057.4:c.*343+103_*343+105del	ENSP00000481988.1:n.*343+103_*343+105del
NM_000465.3:c.1677+103_1677+105del	NP_000456.2:n.1677+103_1677+105del
NM_001282543.1:c.1620+103_1620+105del	NP_001269472.1:n.1620+103_1620+105del
NM_001282545.1:c.324+103_324+105del	NP_001269474.1:n.324+103_324+105del
NM_001282548.1:c.267+103_267+105del	NP_001269477.1:n.267+103_267+105del
NM_001282549.1:c.365-21836_365-21834del	NP_001269478.1:n.365-21836_365-21834del
NR_104212.1:n.1670+103_1670+105del
NR_104215.1:n.1613+103_1613+105del
NR_104216.1:n.869+103_869+105del
XM_011511567.1:c.1623+103_1623+105del	XP_011509869.1:n.1623+103_1623+105del
XM_011511568.1:c.1677+103_1677+105del	XP_011509870.1:n.1677+103_1677+105del
XM_017004613.1:c.1776+103_1776+105del	XP_016860102.1:n.1776+103_1776+105del
XM_017004614.1:c.1776+103_1776+105del	XP_016860103.1:n.1776+103_1776+105del
XR_002959322.1:n.1867+103_1867+105del
NM_000465.4:c.1677+103_1677+105del MANE Select	NP_000456.2:n.1677+103_1677+105del
NM_001282543.2:c.1620+103_1620+105del	NP_001269472.1:n.1620+103_1620+105del
NM_001282545.2:c.324+103_324+105del	NP_001269474.1:n.324+103_324+105del
NM_001282548.2:c.267+103_267+105del	NP_001269477.1:n.267+103_267+105del
NM_001282549.2:c.365-21836_365-21834del	NP_001269478.1:n.365-21836_365-21834del
NR_104212.2:n.1642+103_1642+105del
NR_104215.2:n.1585+103_1585+105del
NR_104216.2:n.841+103_841+105del