Canonical Allele Identifier: CA2759859936

Gene: TP63

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.189890721_189890723del , CM000665.2:g.189890721_189890723del	GRCh38
NC_000003.11:g.189608510_189608512del , CM000665.1:g.189608510_189608512del	GRCh37
NC_000003.10:g.191091204_191091206del	NCBI36
NG_007550.1:g.264295_264297del
NG_007550.2:g.264295_264297del
NG_007550.3:g.298976_298978del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264731.8:c.1653-68_1653-66del MANE Select	ENSP00000264731.3:n.1653-68_1653-66del
ENST00000354600.10:c.1371-68_1371-66del MANE Plus Clinical	ENSP00000346614.5:n.1371-68_1371-66del
ENST00000264731.7:c.1653-68_1653-66del	ENSP00000264731.3:n.1653-68_1653-66del
ENST00000320472.9:c.1508-3485_1508-3483del	ENSP00000317510.5:n.1508-3485_1508-3483del
ENST00000354600.9:c.1371-68_1371-66del	ENSP00000346614.5:n.1371-68_1371-66del
ENST00000392460.7:c.1652+1237_1652+1239del	ENSP00000376253.3:n.1652+1237_1652+1239del
ENST00000392461.7:c.1226-3485_1226-3483del	ENSP00000376254.3:n.1226-3485_1226-3483del
ENST00000392463.6:c.1370+1237_1370+1239del	ENSP00000376256.2:n.1370+1237_1370+1239del
ENST00000440651.6:c.1641-68_1641-66del	ENSP00000394337.2:n.1641-68_1641-66del
ENST00000449992.5:c.1116-68_1116-66del	ENSP00000387839.1:n.1116-68_1116-66del
ENST00000456148.1:c.1359-68_1359-66del	ENSP00000389485.1:n.1359-68_1359-66del
NM_001114978.1:c.1652+1237_1652+1239del	NP_001108450.1:n.1652+1237_1652+1239del
NM_001114980.1:c.1371-68_1371-66del	NP_001108452.1:n.1371-68_1371-66del
NM_001114981.1:c.1370+1237_1370+1239del	NP_001108453.1:n.1370+1237_1370+1239del
NM_003722.4:c.1653-68_1653-66del	NP_003713.3:n.1653-68_1653-66del
XM_005247843.2:c.1641-68_1641-66del	XP_005247900.1:n.1641-68_1641-66del
XM_005247844.3:c.1602-68_1602-66del	XP_005247901.1:n.1602-68_1602-66del
XM_011513251.1:c.1650-68_1650-66del	XP_011511553.1:n.1650-68_1650-66del
XM_011513252.1:c.1647-68_1647-66del	XP_011511554.1:n.1647-68_1647-66del
XM_011513253.1:c.1614-68_1614-66del	XP_011511555.1:n.1614-68_1614-66del
NM_001329144.1:c.1508-3485_1508-3483del	NP_001316073.1:n.1508-3485_1508-3483del
NM_001329145.1:c.1226-3485_1226-3483del	NP_001316074.1:n.1226-3485_1226-3483del
NM_001329146.1:c.1116-68_1116-66del	NP_001316075.1:n.1116-68_1116-66del
NM_001329148.1:c.1641-68_1641-66del	NP_001316077.1:n.1641-68_1641-66del
NM_001329149.1:c.1214-3485_1214-3483del	NP_001316078.1:n.1214-3485_1214-3483del
NM_001329150.1:c.959-3485_959-3483del	NP_001316079.1:n.959-3485_959-3483del
NM_001329964.1:c.1647-68_1647-66del	NP_001316893.1:n.1647-68_1647-66del
NM_003722.5:c.1653-68_1653-66del MANE Select	NP_003713.3:n.1653-68_1653-66del
NM_001114978.2:c.1652+1237_1652+1239del	NP_001108450.1:n.1652+1237_1652+1239del
NM_001114980.2:c.1371-68_1371-66del MANE Plus Clinical	NP_001108452.1:n.1371-68_1371-66del
NM_001114981.2:c.1370+1237_1370+1239del	NP_001108453.1:n.1370+1237_1370+1239del
NM_001329144.2:c.1508-3485_1508-3483del	NP_001316073.1:n.1508-3485_1508-3483del
NM_001329145.2:c.1226-3485_1226-3483del	NP_001316074.1:n.1226-3485_1226-3483del
NM_001329146.2:c.1116-68_1116-66del	NP_001316075.1:n.1116-68_1116-66del
NM_001329148.2:c.1641-68_1641-66del	NP_001316077.1:n.1641-68_1641-66del
NM_001329149.2:c.1214-3485_1214-3483del	NP_001316078.1:n.1214-3485_1214-3483del
NM_001329150.2:c.959-3485_959-3483del	NP_001316079.1:n.959-3485_959-3483del
NM_001329964.2:c.1647-68_1647-66del	NP_001316893.1:n.1647-68_1647-66del