Canonical Allele Identifier: CA476144850

Linked Data

MyVariant Identifiers: chr11:g.86663503del (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952463del , CM000673.2:g.86952463del GRCh38
NC_000011.9:g.86663505del , CM000673.1:g.86663505del GRCh37
NC_000011.8:g.86341153del NCBI36
NG_011752.1:g.7931del

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.295del (FZD4) MANE Select ENSP00000434034.1:p.Cys99ValfsTer?
ENST00000531380.1:c.295del (FZD4) ENSP00000434034.1:p.Cys99ValfsTer?
ENST00000532234.5:c.*1456del (PRSS23) ENSP00000436676.1:n.*1456del
ENST00000533902.2:c.*1178del (PRSS23) ENSP00000437268.1:n.*1178del
NM_012193.3:c.295del (FZD4) NP_036325.2:p.Cys99ValfsTer?
NR_120591.1:n.2128del (PRSS23)
NR_120592.1:n.1877del (PRSS23)
NR_120591.2:n.1826del (PRSS23)
NR_120592.2:n.1575del (PRSS23)
NM_012193.4:c.295del (FZD4) MANE Select NP_036325.2:p.Cys99ValfsTer?
NR_120591.3:n.1826del (PRSS23)