Canonical Allele Identifier: CA2669044228

Gene: TP63

Linked Data

• gnomAD v4: 3-189890752-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.189890752T>C , CM000665.2:g.189890752T>C	GRCh38
NC_000003.11:g.189608541T>C , CM000665.1:g.189608541T>C	GRCh37
NC_000003.10:g.191091235T>C	NCBI36
NG_007550.1:g.264326T>C
NG_007550.2:g.264326T>C
NG_007550.3:g.299007T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000264731.8:c.1653-37T>C MANE Select	ENSP00000264731.3:n.1653-37T>C
ENST00000354600.10:c.1371-37T>C MANE Plus Clinical	ENSP00000346614.5:n.1371-37T>C
ENST00000264731.7:c.1653-37T>C	ENSP00000264731.3:n.1653-37T>C
ENST00000320472.9:c.1508-3454T>C	ENSP00000317510.5:n.1508-3454T>C
ENST00000354600.9:c.1371-37T>C	ENSP00000346614.5:n.1371-37T>C
ENST00000392460.7:c.1652+1268T>C	ENSP00000376253.3:n.1652+1268T>C
ENST00000392461.7:c.1226-3454T>C	ENSP00000376254.3:n.1226-3454T>C
ENST00000392463.6:c.1370+1268T>C	ENSP00000376256.2:n.1370+1268T>C
ENST00000440651.6:c.1641-37T>C	ENSP00000394337.2:n.1641-37T>C
ENST00000449992.5:c.1116-37T>C	ENSP00000387839.1:n.1116-37T>C
ENST00000456148.1:c.1359-37T>C	ENSP00000389485.1:n.1359-37T>C
NM_001114978.1:c.1652+1268T>C	NP_001108450.1:n.1652+1268T>C
NM_001114980.1:c.1371-37T>C	NP_001108452.1:n.1371-37T>C
NM_001114981.1:c.1370+1268T>C	NP_001108453.1:n.1370+1268T>C
NM_003722.4:c.1653-37T>C	NP_003713.3:n.1653-37T>C
XM_005247843.2:c.1641-37T>C	XP_005247900.1:n.1641-37T>C
XM_005247844.3:c.1602-37T>C	XP_005247901.1:n.1602-37T>C
XM_011513251.1:c.1650-37T>C	XP_011511553.1:n.1650-37T>C
XM_011513252.1:c.1647-37T>C	XP_011511554.1:n.1647-37T>C
XM_011513253.1:c.1614-37T>C	XP_011511555.1:n.1614-37T>C
NM_001329144.1:c.1508-3454T>C	NP_001316073.1:n.1508-3454T>C
NM_001329145.1:c.1226-3454T>C	NP_001316074.1:n.1226-3454T>C
NM_001329146.1:c.1116-37T>C	NP_001316075.1:n.1116-37T>C
NM_001329148.1:c.1641-37T>C	NP_001316077.1:n.1641-37T>C
NM_001329149.1:c.1214-3454T>C	NP_001316078.1:n.1214-3454T>C
NM_001329150.1:c.959-3454T>C	NP_001316079.1:n.959-3454T>C
NM_001329964.1:c.1647-37T>C	NP_001316893.1:n.1647-37T>C
NM_003722.5:c.1653-37T>C MANE Select	NP_003713.3:n.1653-37T>C
NM_001114978.2:c.1652+1268T>C	NP_001108450.1:n.1652+1268T>C
NM_001114980.2:c.1371-37T>C MANE Plus Clinical	NP_001108452.1:n.1371-37T>C
NM_001114981.2:c.1370+1268T>C	NP_001108453.1:n.1370+1268T>C
NM_001329144.2:c.1508-3454T>C	NP_001316073.1:n.1508-3454T>C
NM_001329145.2:c.1226-3454T>C	NP_001316074.1:n.1226-3454T>C
NM_001329146.2:c.1116-37T>C	NP_001316075.1:n.1116-37T>C
NM_001329148.2:c.1641-37T>C	NP_001316077.1:n.1641-37T>C
NM_001329149.2:c.1214-3454T>C	NP_001316078.1:n.1214-3454T>C
NM_001329150.2:c.959-3454T>C	NP_001316079.1:n.959-3454T>C
NM_001329964.2:c.1647-37T>C	NP_001316893.1:n.1647-37T>C