Canonical Allele Identifier: CA1428414173
Gene: TP63 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.189625635A= , CM000665.2:g.189625635A= GRCh38
NC_000003.11:g.189343424A= , CM000665.1:g.189343424A= GRCh37
NC_000003.10:g.190826118A= NCBI36
NG_007550.3:g.33890A=

Transcript Alleles

HGVS Amino-acid Change
NM_001329964.1:c.56+28397A= NP_001316893.1:n.56+28397A=
NM_001329964.2:c.56+28397A= NP_001316893.1:n.56+28397A=
XM_011513251.1:c.59+2318A= XP_011511553.1:n.59+2318A=
XM_011513252.1:c.56+28397A= XP_011511554.1:n.56+28397A=
XM_011513253.1:c.23+58740A= XP_011511555.1:n.23+58740A=