Canonical Allele Identifier: CA355751333

Gene: TP63

Linked Data

• dbSNP Id: rs2108873652
• MyVariant Identifiers: chr3:g.189612097C>G (hg19) ; chr3:g.189894308C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.189894308C>G , CM000665.2:g.189894308C>G	GRCh38
NC_000003.11:g.189612097C>G , CM000665.1:g.189612097C>G	GRCh37
NC_000003.10:g.191094791C>G	NCBI36
NG_007550.1:g.267882C>G
NG_007550.2:g.267882C>G
NG_007550.3:g.302563C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000264731.8:c.1849C>G MANE Select	ENSP00000264731.3:p.Leu617Val
ENST00000354600.10:c.1567C>G MANE Plus Clinical	ENSP00000346614.5:p.Leu523Val
ENST00000264731.7:c.1849C>G	ENSP00000264731.3:p.Leu617Val
ENST00000320472.9:c.*77C>G	ENSP00000317510.5:n.*77C>G
ENST00000354600.9:c.1567C>G	ENSP00000346614.5:p.Leu523Val
ENST00000440651.6:c.1837C>G	ENSP00000394337.2:p.Leu613Val
ENST00000449992.5:c.1312C>G	ENSP00000387839.1:p.Leu438Val
ENST00000456148.1:c.1555C>G	ENSP00000389485.1:p.Leu519Val
NM_001114978.1:c.*87C>G	NP_001108450.1:n.*87C>G
NM_001114980.1:c.1567C>G	NP_001108452.1:p.Leu523Val
NM_001114981.1:c.*87C>G	NP_001108453.1:n.*87C>G
NM_003722.4:c.1849C>G	NP_003713.3:p.Leu617Val
XM_005247843.2:c.1837C>G	XP_005247900.1:p.Leu613Val
XM_005247844.3:c.1798C>G	XP_005247901.1:p.Leu600Val
XM_011513251.1:c.1846C>G	XP_011511553.1:p.Leu616Val
XM_011513252.1:c.1843C>G	XP_011511554.1:p.Leu615Val
XM_011513253.1:c.1810C>G	XP_011511555.1:p.Leu604Val
NM_001329144.1:c.*77C>G	NP_001316073.1:n.*77C>G
NM_001329145.1:c.*77C>G	NP_001316074.1:n.*77C>G
NM_001329146.1:c.1312C>G	NP_001316075.1:p.Leu438Val
NM_001329148.1:c.1837C>G	NP_001316077.1:p.Leu613Val
NM_001329149.1:c.*77C>G	NP_001316078.1:n.*77C>G
NM_001329150.1:c.*77C>G	NP_001316079.1:n.*77C>G
NM_001329964.1:c.1843C>G	NP_001316893.1:p.Leu615Val
NM_003722.5:c.1849C>G MANE Select	NP_003713.3:p.Leu617Val
NM_001114978.2:c.*87C>G	NP_001108450.1:n.*87C>G
NM_001114980.2:c.1567C>G MANE Plus Clinical	NP_001108452.1:p.Leu523Val
NM_001114981.2:c.*87C>G	NP_001108453.1:n.*87C>G
NM_001329144.2:c.*77C>G	NP_001316073.1:n.*77C>G
NM_001329145.2:c.*77C>G	NP_001316074.1:n.*77C>G
NM_001329146.2:c.1312C>G	NP_001316075.1:p.Leu438Val
NM_001329148.2:c.1837C>G	NP_001316077.1:p.Leu613Val
NM_001329149.2:c.*77C>G	NP_001316078.1:n.*77C>G
NM_001329150.2:c.*77C>G	NP_001316079.1:n.*77C>G
NM_001329964.2:c.1843C>G	NP_001316893.1:p.Leu615Val