Canonical Allele Identifier: CA2752159

Gene: TP63

Linked Data

• dbSNP Id: rs747443275
• ExAC: 3:189526265 T / G
• gnomAD v2: 3-189526265-T-G
• gnomAD v4: 3-189808476-T-G
• MyVariant Identifiers: chr3:g.189526265T>G (hg19) ; chr3:g.189808476T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.189808476T>G , CM000665.2:g.189808476T>G	GRCh38
NC_000003.11:g.189526265T>G , CM000665.1:g.189526265T>G	GRCh37
NC_000003.10:g.191008959T>G	NCBI36
NG_007550.1:g.182050T>G
NG_007550.2:g.182050T>G
NG_007550.3:g.216731T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264731.8:c.529T>G MANE Select	ENSP00000264731.3:p.Phe177Val
ENST00000354600.10:c.247T>G MANE Plus Clinical	ENSP00000346614.5:p.Phe83Val
ENST00000264731.7:c.529T>G	ENSP00000264731.3:p.Phe177Val
ENST00000320472.9:c.529T>G	ENSP00000317510.5:p.Phe177Val
ENST00000354600.9:c.247T>G	ENSP00000346614.5:p.Phe83Val
ENST00000392460.7:c.529T>G	ENSP00000376253.3:p.Phe177Val
ENST00000392461.7:c.247T>G	ENSP00000376254.3:p.Phe83Val
ENST00000392463.6:c.247T>G	ENSP00000376256.2:p.Phe83Val
ENST00000418709.6:c.529T>G	ENSP00000407144.2:p.Phe177Val
ENST00000434928.5:c.247T>G	ENSP00000401661.1:p.Phe83Val
ENST00000437221.5:c.247T>G	ENSP00000392488.1:p.Phe83Val
ENST00000440651.6:c.529T>G	ENSP00000394337.2:p.Phe177Val
ENST00000449992.5:c.42+18634T>G	ENSP00000387839.1:n.42+18634T>G
ENST00000456148.1:c.247T>G	ENSP00000389485.1:p.Phe83Val
ENST00000460036.1:n.353T>G
NM_001114978.1:c.529T>G	NP_001108450.1:p.Phe177Val
NM_001114979.1:c.529T>G	NP_001108451.1:p.Phe177Val
NM_001114980.1:c.247T>G	NP_001108452.1:p.Phe83Val
NM_001114981.1:c.247T>G	NP_001108453.1:p.Phe83Val
NM_001114982.1:c.247T>G	NP_001108454.1:p.Phe83Val
NM_003722.4:c.529T>G	NP_003713.3:p.Phe177Val
XM_005247843.2:c.529T>G	XP_005247900.1:p.Phe177Val
XM_005247844.3:c.478T>G	XP_005247901.1:p.Phe160Val
XM_005247846.2:c.529T>G	XP_005247903.1:p.Phe177Val
XM_011513251.1:c.526T>G	XP_011511553.1:p.Phe176Val
XM_011513252.1:c.523T>G	XP_011511554.1:p.Phe175Val
XM_011513253.1:c.490T>G	XP_011511555.1:p.Phe164Val
NM_001329144.1:c.529T>G	NP_001316073.1:p.Phe177Val
NM_001329145.1:c.247T>G	NP_001316074.1:p.Phe83Val
NM_001329146.1:c.42+18634T>G	NP_001316075.1:n.42+18634T>G
NM_001329148.1:c.529T>G	NP_001316077.1:p.Phe177Val
NM_001329149.1:c.247T>G	NP_001316078.1:p.Phe83Val
NM_001329150.1:c.42+18634T>G	NP_001316079.1:n.42+18634T>G
NM_001329964.1:c.523T>G	NP_001316893.1:p.Phe175Val
NM_003722.5:c.529T>G MANE Select	NP_003713.3:p.Phe177Val
NM_001114978.2:c.529T>G	NP_001108450.1:p.Phe177Val
NM_001114979.2:c.529T>G	NP_001108451.1:p.Phe177Val
NM_001114980.2:c.247T>G MANE Plus Clinical	NP_001108452.1:p.Phe83Val
NM_001114981.2:c.247T>G	NP_001108453.1:p.Phe83Val
NM_001114982.2:c.247T>G	NP_001108454.1:p.Phe83Val
NM_001329144.2:c.529T>G	NP_001316073.1:p.Phe177Val
NM_001329145.2:c.247T>G	NP_001316074.1:p.Phe83Val
NM_001329146.2:c.42+18634T>G	NP_001316075.1:n.42+18634T>G
NM_001329148.2:c.529T>G	NP_001316077.1:p.Phe177Val
NM_001329149.2:c.247T>G	NP_001316078.1:p.Phe83Val
NM_001329150.2:c.42+18634T>G	NP_001316079.1:n.42+18634T>G
NM_001329964.2:c.523T>G	NP_001316893.1:p.Phe175Val