Canonical Allele Identifier: CA2695215100

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951257_86951267del , CM000673.2:g.86951257_86951267del GRCh38
NC_000011.9:g.86662299_86662309del , CM000673.1:g.86662299_86662309del GRCh37
NC_000011.8:g.86339947_86339957del NCBI36
NG_011752.1:g.9128_9138del

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.1492_1502del (FZD4) MANE Select ENSP00000434034.1:p.Ala498SerfsTer?
ENST00000528769.5:n.314_324del (PRSS23)
ENST00000531380.1:c.1492_1502del (FZD4) ENSP00000434034.1:p.Ala498SerfsTer?
ENST00000531521.1:n.428_438del (PRSS23)
ENST00000532234.5:c.*250_*260del (PRSS23) ENSP00000436676.1:n.*250_*260del
ENST00000533902.2:c.248_258del (PRSS23) ENSP00000437268.1:p.Ser83ThrfsTer8
NM_012193.3:c.1492_1502del (FZD4) NP_036325.2:p.Ala498SerfsTer?
NR_120591.1:n.922_932del (PRSS23)
NR_120592.1:n.671_681del (PRSS23)
NR_120591.2:n.620_630del (PRSS23)
NR_120592.2:n.369_379del (PRSS23)
NM_012193.4:c.1492_1502del (FZD4) MANE Select NP_036325.2:p.Ala498SerfsTer?
NR_120591.3:n.620_630del (PRSS23)