Canonical Allele Identifier: CA253501

Linked Data

dbSNP Id: rs80358303

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951256_86951257del , CM000673.2:g.86951256_86951257del GRCh38
NC_000011.9:g.86662298_86662299del , CM000673.1:g.86662298_86662299del GRCh37
NC_000011.8:g.86339946_86339947del NCBI36
NG_011752.1:g.9137_9138del

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.1501_1502del (FZD4) MANE Select ENSP00000434034.1:p.Leu501SerfsTer?
ENST00000528769.5:n.313_314del (PRSS23)
ENST00000531380.1:c.1501_1502del (FZD4) ENSP00000434034.1:p.Leu501SerfsTer?
ENST00000531521.1:n.427_428del (PRSS23)
ENST00000532234.5:c.*249_*250del (PRSS23) ENSP00000436676.1:n.*249_*250del
ENST00000533902.2:c.247_248del (PRSS23) ENSP00000437268.1:p.Ser83PhefsTer11
NM_012193.3:c.1501_1502del (FZD4) NP_036325.2:p.Leu501SerfsTer?
NR_120591.1:n.921_922del (PRSS23)
NR_120592.1:n.670_671del (PRSS23)
NR_120591.2:n.619_620del (PRSS23)
NR_120592.2:n.368_369del (PRSS23)
NM_012193.4:c.1501_1502del (FZD4) MANE Select NP_036325.2:p.Leu501SerfsTer?
NR_120591.3:n.619_620del (PRSS23)