Canonical Allele Identifier: CA645590559

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952460del , CM000673.2:g.86952460del GRCh38
NC_000011.9:g.86663502del , CM000673.1:g.86663502del GRCh37
NC_000011.8:g.86341150del NCBI36
NG_011752.1:g.7932del

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.296del (FZD4) MANE Select ENSP00000434034.1:p.Cys99PhefsTer?
ENST00000531380.1:c.296del (FZD4) ENSP00000434034.1:p.Cys99PhefsTer?
ENST00000532234.5:c.*1453del (PRSS23) ENSP00000436676.1:n.*1453del
ENST00000533902.2:c.*1175del (PRSS23) ENSP00000437268.1:n.*1175del
NM_012193.3:c.296del (FZD4) NP_036325.2:p.Cys99PhefsTer?
NR_120591.1:n.2125del (PRSS23)
NR_120592.1:n.1874del (PRSS23)
NR_120591.2:n.1823del (PRSS23)
NR_120592.2:n.1572del (PRSS23)
NM_012193.4:c.296del (FZD4) MANE Select NP_036325.2:p.Cys99PhefsTer?
NR_120591.3:n.1823del (PRSS23)