Canonical Allele Identifier: CA409433411

Gene: ZBP1

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.57615578C>G , CM000682.2:g.57615578C>G	GRCh38
NC_000020.10:g.56190634C>G , CM000682.1:g.56190634C>G	GRCh37
NC_000020.9:g.55624040C>G	NCBI36
NG_031836.1:g.9999G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371173.8:c.262G>C MANE Select	ENSP00000360215.3:p.Glu88Gln
ENST00000371173.7:c.262G>C	ENSP00000360215.3:p.Glu88Gln
ENST00000395822.7:c.37G>C	ENSP00000379167.3:p.Glu13Gln
ENST00000432548.2:n.457G>C
ENST00000461547.5:n.2504G>C
ENST00000480037.1:n.1057G>C
ENST00000538947.5:n.488G>C
ENST00000541799.1:c.262G>C	ENSP00000440552.1:p.Glu88Gln
ENST00000546110.5:n.222G>C
NM_001160417.1:c.262G>C	NP_001153889.1:p.Glu88Gln
NM_001160418.1:c.37G>C	NP_001153890.1:p.Glu13Gln
NM_001160419.2:c.262G>C	NP_001153891.1:p.Glu88Gln
NM_030776.2:c.262G>C	NP_110403.2:p.Glu88Gln
XM_011529057.1:c.262G>C	XP_011527359.1:p.Glu88Gln
XM_011529058.1:c.262G>C	XP_011527360.1:p.Glu88Gln
XM_011529059.1:c.262G>C	XP_011527361.1:p.Glu88Gln
XR_936633.1:n.393G>C
XR_936634.1:n.393G>C
XR_936636.1:n.393G>C
XR_936637.1:n.488G>C
XR_936638.1:n.393G>C
XR_936639.1:n.318G>C
XR_936640.1:n.222G>C
NM_001323966.1:c.37G>C	NP_001310895.1:p.Glu13Gln
NR_136660.1:n.318G>C
XM_011529057.2:c.262G>C	XP_011527359.1:p.Glu88Gln
XM_011529058.2:c.262G>C	XP_011527360.1:p.Glu88Gln
XM_017028086.1:c.262G>C	XP_016883575.1:p.Glu88Gln
XR_001754408.1:n.393G>C
XR_001754409.1:n.393G>C
XR_001754410.1:n.393G>C
XR_001754412.1:n.488G>C
XR_001754413.1:n.393G>C
XR_001754414.1:n.222G>C
XR_001754415.1:n.393G>C
NM_030776.3:c.262G>C MANE Select	NP_110403.2:p.Glu88Gln
NM_001160417.2:c.262G>C	NP_001153889.1:p.Glu88Gln
NM_001160418.2:c.37G>C	NP_001153890.1:p.Glu13Gln
NM_001160419.3:c.262G>C	NP_001153891.1:p.Glu88Gln
NM_001323966.2:c.37G>C	NP_001310895.1:p.Glu13Gln
NR_136660.2:n.168G>C