Canonical Allele Identifier: CA735405396

Gene: TP73

Linked Data - Predicted Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.3695328G>T , CM000663.2:g.3695328G>T	GRCh38
NC_000001.10:g.3611892G>T , CM000663.1:g.3611892G>T	GRCh37
NC_000001.9:g.3601752G>T	NCBI36
NG_017035.2:g.47764G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000603362.6:c.186+12148G>T	ENSP00000474626.1:n.186+12148G>T
ENST00000604479.6:c.186+12148G>T	ENSP00000474322.1:n.186+12148G>T
ENST00000713570.1:c.186+12148G>T	ENSP00000518863.1:n.186+12148G>T
ENST00000713571.1:n.298+12148G>T
ENST00000713572.1:c.186+12148G>T	ENSP00000518864.1:n.186+12148G>T
ENST00000378295.9:c.186+12148G>T MANE Select	ENSP00000367545.4:n.186+12148G>T
ENST00000346387.8:c.186+12148G>T	ENSP00000340740.4:n.186+12148G>T
ENST00000354437.8:c.186+12148G>T	ENSP00000346423.4:n.186+12148G>T
ENST00000357733.7:c.186+12148G>T	ENSP00000350366.3:n.186+12148G>T
ENST00000378280.5:c.39+4384G>T	ENSP00000367529.1:n.39+4384G>T
ENST00000378285.5:c.39+4384G>T	ENSP00000367534.1:n.39+4384G>T
ENST00000378288.8:c.39+4384G>T	ENSP00000367537.4:n.39+4384G>T
ENST00000378295.8:c.186+12148G>T	ENSP00000367545.4:n.186+12148G>T
ENST00000603362.5:c.186+12148G>T	ENSP00000474626.1:n.186+12148G>T
ENST00000603364.5:n.238+4384G>T
ENST00000604074.5:c.186+12148G>T	ENSP00000475143.1:n.186+12148G>T
ENST00000604479.5:c.186+12148G>T	ENSP00000474322.1:n.186+12148G>T
NM_001126240.2:c.39+4384G>T	NP_001119712.1:n.39+4384G>T
NM_001126241.2:c.39+4384G>T	NP_001119713.1:n.39+4384G>T
NM_001126242.2:c.39+4384G>T	NP_001119714.1:n.39+4384G>T
NM_001204184.1:c.186+12148G>T	NP_001191113.1:n.186+12148G>T
NM_001204185.1:c.186+12148G>T	NP_001191114.1:n.186+12148G>T
NM_001204186.1:c.186+12148G>T	NP_001191115.1:n.186+12148G>T
NM_001204187.1:c.186+12148G>T	NP_001191116.1:n.186+12148G>T
NM_001204188.1:c.186+12148G>T	NP_001191117.1:n.186+12148G>T
NM_001204189.1:c.39+4384G>T	NP_001191118.1:n.39+4384G>T
NM_001204190.1:c.39+4384G>T	NP_001191119.1:n.39+4384G>T
NM_001204191.1:c.39+4384G>T	NP_001191120.1:n.39+4384G>T
NM_005427.3:c.186+12148G>T	NP_005418.1:n.186+12148G>T
XM_011542064.1:c.186+12148G>T	XP_011540366.1:n.186+12148G>T
NM_005427.4:c.186+12148G>T MANE Select	NP_005418.1:n.186+12148G>T
NM_001126240.3:c.39+4384G>T	NP_001119712.1:n.39+4384G>T
NM_001126241.3:c.39+4384G>T	NP_001119713.1:n.39+4384G>T
NM_001126242.3:c.39+4384G>T	NP_001119714.1:n.39+4384G>T
NM_001204184.2:c.186+12148G>T	NP_001191113.1:n.186+12148G>T
NM_001204185.2:c.186+12148G>T	NP_001191114.1:n.186+12148G>T
NM_001204186.2:c.186+12148G>T	NP_001191115.1:n.186+12148G>T
NM_001204189.2:c.39+4384G>T	NP_001191118.1:n.39+4384G>T
NM_001204190.2:c.39+4384G>T	NP_001191119.1:n.39+4384G>T
NM_001204191.2:c.39+4384G>T	NP_001191120.1:n.39+4384G>T
NM_001204187.2:c.186+12148G>T	NP_001191116.1:n.186+12148G>T
NM_001204188.2:c.186+12148G>T	NP_001191117.1:n.186+12148G>T