Canonical Allele Identifier: CA548733264

Gene: TP63

Linked Data

• dbSNP Id: rs1470665726
• gnomAD v2: 3-189356189-G-GTACAAGT
• gnomAD v3: 3-189638400-G-GTACAAGT
• gnomAD v4: 3-189638400-G-GTACAAGT
• MyVariant Identifiers: chr3:g.189356189_189356190insTACAAGT (hg19) ; chr3:g.189638400_189638401insTACAAGT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.189638401_189638402insACAAGTT , CM000665.2:g.189638401_189638402insACAAGTT	GRCh38
NC_000003.11:g.189356190_189356191insACAAGTT , CM000665.1:g.189356190_189356191insACAAGTT	GRCh37
NC_000003.10:g.190838884_190838885insACAAGTT	NCBI36
NG_007550.1:g.11975_11976insACAAGTT
NG_007550.2:g.11975_11976insACAAGTT
NG_007550.3:g.46656_46657insACAAGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264731.8:c.62+6824_62+6825insACAAGTT MANE Select	ENSP00000264731.3:n.62+6824_62+6825insACAAGTT
ENST00000264731.7:c.62+6824_62+6825insACAAGTT	ENSP00000264731.3:n.62+6824_62+6825insACAAGTT
ENST00000320472.9:c.62+6824_62+6825insACAAGTT	ENSP00000317510.5:n.62+6824_62+6825insACAAGTT
ENST00000392460.7:c.62+6824_62+6825insACAAGTT	ENSP00000376253.3:n.62+6824_62+6825insACAAGTT
ENST00000418709.6:c.62+6824_62+6825insACAAGTT	ENSP00000407144.2:n.62+6824_62+6825insACAAGTT
ENST00000440651.6:c.62+6824_62+6825insACAAGTT	ENSP00000394337.2:n.62+6824_62+6825insACAAGTT
ENST00000486398.1:n.162+6824_162+6825insACAAGTT
NM_001114978.1:c.62+6824_62+6825insACAAGTT	NP_001108450.1:n.62+6824_62+6825insACAAGTT
NM_001114979.1:c.62+6824_62+6825insACAAGTT	NP_001108451.1:n.62+6824_62+6825insACAAGTT
NM_003722.4:c.62+6824_62+6825insACAAGTT	NP_003713.3:n.62+6824_62+6825insACAAGTT
XM_005247843.2:c.62+6824_62+6825insACAAGTT	XP_005247900.1:n.62+6824_62+6825insACAAGTT
XM_005247844.3:c.11+7126_11+7127insACAAGTT	XP_005247901.1:n.11+7126_11+7127insACAAGTT
XM_005247846.2:c.62+6824_62+6825insACAAGTT	XP_005247903.1:n.62+6824_62+6825insACAAGTT
XM_011513251.1:c.59+15084_59+15085insACAAGTT	XP_011511553.1:n.59+15084_59+15085insACAAGTT
XM_011513252.1:c.56+41163_56+41164insACAAGTT	XP_011511554.1:n.56+41163_56+41164insACAAGTT
XM_011513253.1:c.23+71506_23+71507insACAAGTT	XP_011511555.1:n.23+71506_23+71507insACAAGTT
NM_001329144.1:c.62+6824_62+6825insACAAGTT	NP_001316073.1:n.62+6824_62+6825insACAAGTT
NM_001329148.1:c.62+6824_62+6825insACAAGTT	NP_001316077.1:n.62+6824_62+6825insACAAGTT
NM_001329964.1:c.56+41163_56+41164insACAAGTT	NP_001316893.1:n.56+41163_56+41164insACAAGTT
NM_003722.5:c.62+6824_62+6825insACAAGTT MANE Select	NP_003713.3:n.62+6824_62+6825insACAAGTT
NM_001114978.2:c.62+6824_62+6825insACAAGTT	NP_001108450.1:n.62+6824_62+6825insACAAGTT
NM_001114979.2:c.62+6824_62+6825insACAAGTT	NP_001108451.1:n.62+6824_62+6825insACAAGTT
NM_001329144.2:c.62+6824_62+6825insACAAGTT	NP_001316073.1:n.62+6824_62+6825insACAAGTT
NM_001329148.2:c.62+6824_62+6825insACAAGTT	NP_001316077.1:n.62+6824_62+6825insACAAGTT
NM_001329964.2:c.56+41163_56+41164insACAAGTT	NP_001316893.1:n.56+41163_56+41164insACAAGTT