Canonical Allele Identifier: CA2615461574

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951435dup , CM000673.2:g.86951435dup GRCh38
NC_000011.9:g.86662477dup , CM000673.1:g.86662477dup GRCh37
NC_000011.8:g.86340125dup NCBI36
NG_011752.1:g.8957dup

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.1321dup (FZD4) MANE Select ENSP00000434034.1:p.Ser441PhefsTer18
ENST00000531380.1:c.1321dup (FZD4) ENSP00000434034.1:p.Ser441PhefsTer18
ENST00000531521.1:n.606dup (PRSS23)
ENST00000532234.5:c.*428dup (PRSS23) ENSP00000436676.1:n.*428dup
ENST00000533902.2:c.*150dup (PRSS23) ENSP00000437268.1:n.*150dup
NM_012193.3:c.1321dup (FZD4) NP_036325.2:p.Ser441PhefsTer18
NR_120591.1:n.1100dup (PRSS23)
NR_120592.1:n.849dup (PRSS23)
NR_120591.2:n.798dup (PRSS23)
NR_120592.2:n.547dup (PRSS23)
NM_012193.4:c.1321dup (FZD4) MANE Select NP_036325.2:p.Ser441PhefsTer18
NR_120591.3:n.798dup (PRSS23)