Canonical Allele Identifier: CA2615456079

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952368del , CM000673.2:g.86952368del GRCh38
NC_000011.9:g.86663410del , CM000673.1:g.86663410del GRCh37
NC_000011.8:g.86341058del NCBI36
NG_011752.1:g.8026del

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.390del (FZD4) MANE Select ENSP00000434034.1:p.Val131SerfsTer2
ENST00000531380.1:c.390del (FZD4) ENSP00000434034.1:p.Val131SerfsTer2
ENST00000532234.5:c.*1361del (PRSS23) ENSP00000436676.1:n.*1361del
ENST00000533902.2:c.*1083del (PRSS23) ENSP00000437268.1:n.*1083del
NM_012193.3:c.390del (FZD4) NP_036325.2:p.Val131SerfsTer2
NR_120591.1:n.2033del (PRSS23)
NR_120592.1:n.1782del (PRSS23)
NR_120591.2:n.1731del (PRSS23)
NR_120592.2:n.1480del (PRSS23)
NM_012193.4:c.390del (FZD4) MANE Select NP_036325.2:p.Val131SerfsTer2
NR_120591.3:n.1731del (PRSS23)