Canonical Allele Identifier: CA2642837978

Gene: TP73

Linked Data

• gnomAD v4: 1-3682355-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.3682355G>T , CM000663.2:g.3682355G>T	GRCh38
NC_000001.10:g.3598919G>T , CM000663.1:g.3598919G>T	GRCh37
NC_000001.9:g.3588779G>T	NCBI36
NG_017035.2:g.34791G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000603362.6:c.-11G>T	ENSP00000474626.1:n.-11G>T
ENST00000604479.6:c.-11G>T	ENSP00000474322.1:n.-11G>T
ENST00000713570.1:c.-11G>T	ENSP00000518863.1:n.-11G>T
ENST00000713571.1:n.102G>T
ENST00000713572.1:c.-11G>T	ENSP00000518864.1:n.-11G>T
ENST00000378295.9:c.-11G>T MANE Select	ENSP00000367545.4:n.-11G>T
ENST00000346387.8:c.-11G>T	ENSP00000340740.4:n.-11G>T
ENST00000354437.8:c.-11G>T	ENSP00000346423.4:n.-11G>T
ENST00000357733.7:c.-11G>T	ENSP00000350366.3:n.-11G>T
ENST00000378295.8:c.-11G>T	ENSP00000367545.4:n.-11G>T
ENST00000604074.5:c.-11G>T	ENSP00000475143.1:n.-11G>T
NM_001204184.1:c.-11G>T	NP_001191113.1:n.-11G>T
NM_001204185.1:c.-11G>T	NP_001191114.1:n.-11G>T
NM_001204186.1:c.-11G>T	NP_001191115.1:n.-11G>T
NM_001204187.1:c.-11G>T	NP_001191116.1:n.-11G>T
NM_001204188.1:c.-11G>T	NP_001191117.1:n.-11G>T
NM_005427.3:c.-11G>T	NP_005418.1:n.-11G>T
XM_011542064.1:c.-11G>T	XP_011540366.1:n.-11G>T
NM_005427.4:c.-11G>T MANE Select	NP_005418.1:n.-11G>T
NM_001204184.2:c.-11G>T	NP_001191113.1:n.-11G>T
NM_001204185.2:c.-11G>T	NP_001191114.1:n.-11G>T
NM_001204186.2:c.-11G>T	NP_001191115.1:n.-11G>T
NM_001204187.2:c.-11G>T	NP_001191116.1:n.-11G>T
NM_001204188.2:c.-11G>T	NP_001191117.1:n.-11G>T