Canonical Allele Identifier: CA624725069

Gene: TP53

Linked Data

• dbSNP Id: rs1567537596
• gnomAD v2: 17-7571550-CTTG-C
• gnomAD v3: 17-7668232-CTTG-C
• gnomAD v4: 17-7668232-CTTG-C
• MyVariant Identifiers: chr17:g.7571551_7571553del (hg19) ; chr17:g.7668233_7668235del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7668237_7668239del , CM000679.2:g.7668237_7668239del	GRCh38
NC_000017.10:g.7571555_7571557del , CM000679.1:g.7571555_7571557del	GRCh37
NC_000017.9:g.7512280_7512282del	NCBI36
NG_017013.2:g.24316_24318del , LRG_321:g.24316_24318del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359597.8:c.994-1991_994-1989del	ENSP00000352610.4:n.994-1991_994-1989del
ENST00000413465.6:c.782+5946_782+5948del	ENSP00000410739.2:n.782+5946_782+5948del
ENST00000635293.1:c.984-810_984-808del	ENSP00000488924.1:n.984-810_984-808del