Canonical Allele Identifier: CA2642847137
Gene: TP73 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.3734753_3734754insTTTTTTAATG , CM000663.2:g.3734753_3734754insTTTTTTAATG GRCh38
NC_000001.10:g.3651317_3651318insTTTTTTAATG , CM000663.1:g.3651317_3651318insTTTTTTAATG GRCh37
NC_000001.9:g.3641177_3641178insTTTTTTAATG NCBI36
NG_017035.2:g.87189_87190insTTTTTTAATG

Transcript Alleles

HGVS Amino-acid change
ENST00000713570.1:c.*1674_*1675insTTTTTTAATG ENSP00000518863.1:n.*1674_*1675insTTTTTTA...
ENST00000713572.1:c.*1674_*1675insTTTTTTAATG ENSP00000518864.1:n.*1674_*1675insTTTTTTA...
ENST00000378295.9:c.*1674_*1675insTTTTTTAATG MANE Select ENSP00000367545.4:n.*1674_*1675insTTTTTTA...
ENST00000346387.8:c.*1674_*1675insTTTTTTAATG ENSP00000340740.4:n.*1674_*1675insTTTTTTA...
ENST00000357733.7:c.*1674_*1675insTTTTTTAATG ENSP00000350366.3:n.*1674_*1675insTTTTTTA...
ENST00000378288.8:c.*1674_*1675insTTTTTTAATG ENSP00000367537.4:n.*1674_*1675insTTTTTTA...
ENST00000378295.8:c.*1674_*1675insTTTTTTAATG ENSP00000367545.4:n.*1674_*1675insTTTTTTA...
ENST00000604074.5:c.*1991_*1992insTTTTTTAATG ENSP00000475143.1:n.*1991_*1992insTTTTTTA...
NM_001126240.2:c.*1674_*1675insTTTTTTAATG NP_001119712.1:n.*1674_*1675insTTTTTTAATG...
NM_001126241.2:c.*1991_*1992insTTTTTTAATG NP_001119713.1:n.*1991_*1992insTTTTTTAATG...
NM_001126242.2:c.*2008_*2009insTTTTTTAATG NP_001119714.1:n.*2008_*2009insTTTTTTAATG...
NM_001204184.1:c.*1991_*1992insTTTTTTAATG NP_001191113.1:n.*1991_*1992insTTTTTTAATG...
NM_001204185.1:c.*2008_*2009insTTTTTTAATG NP_001191114.1:n.*2008_*2009insTTTTTTAATG...
NM_001204186.1:c.*1991_*1992insTTTTTTAATG NP_001191115.1:n.*1991_*1992insTTTTTTAATG...
NM_001204187.1:c.*1674_*1675insTTTTTTAATG NP_001191116.1:n.*1674_*1675insTTTTTTAATG...
NM_001204188.1:c.*1674_*1675insTTTTTTAATG NP_001191117.1:n.*1674_*1675insTTTTTTAATG...
NM_001204189.1:c.*1991_*1992insTTTTTTAATG NP_001191118.1:n.*1991_*1992insTTTTTTAATG...
NM_001204190.1:c.*1674_*1675insTTTTTTAATG NP_001191119.1:n.*1674_*1675insTTTTTTAATG...
NM_001204191.1:c.*1674_*1675insTTTTTTAATG NP_001191120.1:n.*1674_*1675insTTTTTTAATG...
NM_001204192.1:c.*1674_*1675insTTTTTTAATG NP_001191121.1:n.*1674_*1675insTTTTTTAATG...
NM_005427.3:c.*1674_*1675insTTTTTTAATG NP_005418.1:n.*1674_*1675insTTTTTTAATG
XM_011542064.1:c.*1674_*1675insTTTTTTAATG XP_011540366.1:n.*1674_*1675insTTTTTTAATG...
NM_005427.4:c.*1674_*1675insTTTTTTAATG MANE Select NP_005418.1:n.*1674_*1675insTTTTTTAATG
NM_001126240.3:c.*1674_*1675insTTTTTTAATG NP_001119712.1:n.*1674_*1675insTTTTTTAATG...
NM_001126241.3:c.*1991_*1992insTTTTTTAATG NP_001119713.1:n.*1991_*1992insTTTTTTAATG...
NM_001126242.3:c.*2008_*2009insTTTTTTAATG NP_001119714.1:n.*2008_*2009insTTTTTTAATG...
NM_001204184.2:c.*1991_*1992insTTTTTTAATG NP_001191113.1:n.*1991_*1992insTTTTTTAATG...
NM_001204185.2:c.*2008_*2009insTTTTTTAATG NP_001191114.1:n.*2008_*2009insTTTTTTAATG...
NM_001204186.2:c.*1991_*1992insTTTTTTAATG NP_001191115.1:n.*1991_*1992insTTTTTTAATG...
NM_001204189.2:c.*1991_*1992insTTTTTTAATG NP_001191118.1:n.*1991_*1992insTTTTTTAATG...
NM_001204190.2:c.*1674_*1675insTTTTTTAATG NP_001191119.1:n.*1674_*1675insTTTTTTAATG...
NM_001204191.2:c.*1674_*1675insTTTTTTAATG NP_001191120.1:n.*1674_*1675insTTTTTTAATG...
NM_001204192.2:c.*1674_*1675insTTTTTTAATG NP_001191121.1:n.*1674_*1675insTTTTTTAATG...
NM_001204187.2:c.*1674_*1675insTTTTTTAATG NP_001191116.1:n.*1674_*1675insTTTTTTAATG...
NM_001204188.2:c.*1674_*1675insTTTTTTAATG NP_001191117.1:n.*1674_*1675insTTTTTTAATG...