Canonical Allele Identifier: CA1140174352
Gene: TP73 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.3732998G= , CM000663.2:g.3732998G= GRCh38
NC_000001.10:g.3649562G= , CM000663.1:g.3649562G= GRCh37
NC_000001.9:g.3639422G= NCBI36
NG_017035.2:g.85434G=

Transcript Alleles

HGVS Amino-acid Change
NM_005427.4:c.1830G= MANE Select NP_005418.1:p.Ala610=
ENST00000378295.9:c.1830G= MANE Select ENSP00000367545.4:p.Ala610=
NM_001126240.2:c.1683G= NP_001119712.1:p.Ala561=
NM_001126240.3:c.1683G= NP_001119712.1:p.Ala561=
NM_001126241.2:c.*236G= NP_001119713.1:n.*236G=
NM_001126241.3:c.*236G= NP_001119713.1:n.*236G=
NM_001126242.2:c.*253G= NP_001119714.1:n.*253G=
NM_001126242.3:c.*253G= NP_001119714.1:n.*253G=
NM_001204184.1:c.*236G= NP_001191113.1:n.*236G=
NM_001204184.2:c.*236G= NP_001191113.1:n.*236G=
NM_001204185.1:c.*253G= NP_001191114.1:n.*253G=
NM_001204185.2:c.*253G= NP_001191114.1:n.*253G=
NM_001204186.1:c.*236G= NP_001191115.1:n.*236G=
NM_001204186.2:c.*236G= NP_001191115.1:n.*236G=
NM_001204187.1:c.1587G= NP_001191116.1:p.Ala529=
NM_001204187.2:c.1587G= NP_001191116.1:p.Ala529=
NM_001204188.1:c.1542G= NP_001191117.1:p.Ala514=
NM_001204188.2:c.1542G= NP_001191117.1:p.Ala514=
NM_001204189.1:c.*236G= NP_001191118.1:n.*236G=
NM_001204189.2:c.*236G= NP_001191118.1:n.*236G=
NM_001204190.1:c.1440G= NP_001191119.1:p.Ala480=
NM_001204190.2:c.1440G= NP_001191119.1:p.Ala480=
NM_001204191.1:c.1395G= NP_001191120.1:p.Ala465=
NM_001204191.2:c.1395G= NP_001191120.1:p.Ala465=
NM_001204192.1:c.1617G= NP_001191121.1:p.Ala539=
NM_001204192.2:c.1617G= NP_001191121.1:p.Ala539=
NM_005427.3:c.1830G= NP_005418.1:p.Ala610=
ENST00000346387.8:c.1542G= ENSP00000340740.4:p.Ala514=
ENST00000354437.8:c.*236G= ENSP00000346423.4:n.*236G=
ENST00000357733.7:c.1587G= ENSP00000350366.3:p.Ala529=
ENST00000378280.5:c.*253G= ENSP00000367529.1:n.*253G=
ENST00000378285.5:c.*236G= ENSP00000367534.1:n.*236G=
ENST00000378288.8:c.1683G= ENSP00000367537.4:p.Ala561=
ENST00000378290.4:c.1617G= ENSP00000367539.4:p.Ala539=
ENST00000378295.8:c.1830G= ENSP00000367545.4:p.Ala610=
ENST00000603362.5:c.1587G= ENSP00000474626.1:p.Ala529=
ENST00000603362.6:c.1587G= ENSP00000474626.1:p.Ala529=
ENST00000604074.5:c.*236G= ENSP00000475143.1:n.*236G=
ENST00000604479.5:c.1542G= ENSP00000474322.1:p.Ala514=
ENST00000604479.6:c.1542G= ENSP00000474322.1:p.Ala514=
ENST00000604566.1:n.989G=
ENST00000713570.1:c.1830G= ENSP00000518863.1:p.Ala610=
ENST00000713572.1:c.1830G= ENSP00000518864.1:p.Ala610=
XM_011542064.1:c.1830G= XP_011540366.1:p.Ala610=