Canonical Allele Identifier: CA2669044227

Gene: TP63

Linked Data

• gnomAD v4: 3-189890751-TTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.189890753_189890754del , CM000665.2:g.189890753_189890754del	GRCh38
NC_000003.11:g.189608542_189608543del , CM000665.1:g.189608542_189608543del	GRCh37
NC_000003.10:g.191091236_191091237del	NCBI36
NG_007550.1:g.264327_264328del
NG_007550.2:g.264327_264328del
NG_007550.3:g.299008_299009del

Transcript Alleles

HGVS	Amino-acid change
ENST00000264731.8:c.1653-36_1653-35del MANE Select	ENSP00000264731.3:n.1653-36_1653-35del
ENST00000354600.10:c.1371-36_1371-35del MANE Plus Clinical	ENSP00000346614.5:n.1371-36_1371-35del
ENST00000264731.7:c.1653-36_1653-35del	ENSP00000264731.3:n.1653-36_1653-35del
ENST00000320472.9:c.1508-3453_1508-3452del	ENSP00000317510.5:n.1508-3453_1508-3452de...
ENST00000354600.9:c.1371-36_1371-35del	ENSP00000346614.5:n.1371-36_1371-35del
ENST00000392460.7:c.1652+1269_1652+1270del	ENSP00000376253.3:n.1652+1269_1652+1270de...
ENST00000392461.7:c.1226-3453_1226-3452del	ENSP00000376254.3:n.1226-3453_1226-3452de...
ENST00000392463.6:c.1370+1269_1370+1270del	ENSP00000376256.2:n.1370+1269_1370+1270de...
ENST00000440651.6:c.1641-36_1641-35del	ENSP00000394337.2:n.1641-36_1641-35del
ENST00000449992.5:c.1116-36_1116-35del	ENSP00000387839.1:n.1116-36_1116-35del
ENST00000456148.1:c.1359-36_1359-35del	ENSP00000389485.1:n.1359-36_1359-35del
NM_001114978.1:c.1652+1269_1652+1270del	NP_001108450.1:n.1652+1269_1652+1270del
NM_001114980.1:c.1371-36_1371-35del	NP_001108452.1:n.1371-36_1371-35del
NM_001114981.1:c.1370+1269_1370+1270del	NP_001108453.1:n.1370+1269_1370+1270del
NM_003722.4:c.1653-36_1653-35del	NP_003713.3:n.1653-36_1653-35del
XM_005247843.2:c.1641-36_1641-35del	XP_005247900.1:n.1641-36_1641-35del
XM_005247844.3:c.1602-36_1602-35del	XP_005247901.1:n.1602-36_1602-35del
XM_011513251.1:c.1650-36_1650-35del	XP_011511553.1:n.1650-36_1650-35del
XM_011513252.1:c.1647-36_1647-35del	XP_011511554.1:n.1647-36_1647-35del
XM_011513253.1:c.1614-36_1614-35del	XP_011511555.1:n.1614-36_1614-35del
NM_001329144.1:c.1508-3453_1508-3452del	NP_001316073.1:n.1508-3453_1508-3452del
NM_001329145.1:c.1226-3453_1226-3452del	NP_001316074.1:n.1226-3453_1226-3452del
NM_001329146.1:c.1116-36_1116-35del	NP_001316075.1:n.1116-36_1116-35del
NM_001329148.1:c.1641-36_1641-35del	NP_001316077.1:n.1641-36_1641-35del
NM_001329149.1:c.1214-3453_1214-3452del	NP_001316078.1:n.1214-3453_1214-3452del
NM_001329150.1:c.959-3453_959-3452del	NP_001316079.1:n.959-3453_959-3452del
NM_001329964.1:c.1647-36_1647-35del	NP_001316893.1:n.1647-36_1647-35del
NM_003722.5:c.1653-36_1653-35del MANE Select	NP_003713.3:n.1653-36_1653-35del
NM_001114978.2:c.1652+1269_1652+1270del	NP_001108450.1:n.1652+1269_1652+1270del
NM_001114980.2:c.1371-36_1371-35del MANE Plus Clinical	NP_001108452.1:n.1371-36_1371-35del
NM_001114981.2:c.1370+1269_1370+1270del	NP_001108453.1:n.1370+1269_1370+1270del
NM_001329144.2:c.1508-3453_1508-3452del	NP_001316073.1:n.1508-3453_1508-3452del
NM_001329145.2:c.1226-3453_1226-3452del	NP_001316074.1:n.1226-3453_1226-3452del
NM_001329146.2:c.1116-36_1116-35del	NP_001316075.1:n.1116-36_1116-35del
NM_001329148.2:c.1641-36_1641-35del	NP_001316077.1:n.1641-36_1641-35del
NM_001329149.2:c.1214-3453_1214-3452del	NP_001316078.1:n.1214-3453_1214-3452del
NM_001329150.2:c.959-3453_959-3452del	NP_001316079.1:n.959-3453_959-3452del
NM_001329964.2:c.1647-36_1647-35del	NP_001316893.1:n.1647-36_1647-35del