Canonical Allele Identifier: CA225380482

Linked Data

dbSNP Id: rs377030377

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951330dup , CM000673.2:g.86951330dup GRCh38
NC_000011.9:g.86662372dup , CM000673.1:g.86662372dup GRCh37
NC_000011.8:g.86340020dup NCBI36
NG_011752.1:g.9062dup

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.1426dup (FZD4) MANE Select ENSP00000434034.1:p.Val476GlyfsTer2
ENST00000528769.5:n.387dup (PRSS23)
ENST00000531380.1:c.1426dup (FZD4) ENSP00000434034.1:p.Val476GlyfsTer2
ENST00000531521.1:n.501dup (PRSS23)
ENST00000532234.5:c.*323dup (PRSS23) ENSP00000436676.1:n.*323dup
ENST00000533902.2:c.*45dup (PRSS23) ENSP00000437268.1:n.*45dup
NM_012193.3:c.1426dup (FZD4) NP_036325.2:p.Val476GlyfsTer2
NR_120591.1:n.995dup (PRSS23)
NR_120592.1:n.744dup (PRSS23)
NR_120591.2:n.693dup (PRSS23)
NR_120592.2:n.442dup (PRSS23)
NM_012193.4:c.1426dup (FZD4) MANE Select NP_036325.2:p.Val476GlyfsTer2
NR_120591.3:n.693dup (PRSS23)