Canonical Allele Identifier: CA2615456032

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952336dup , CM000673.2:g.86952336dup GRCh38
NC_000011.9:g.86663378dup , CM000673.1:g.86663378dup GRCh37
NC_000011.8:g.86341026dup NCBI36
NG_011752.1:g.8056dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.420dup (FZD4) MANE Select ENSP00000434034.1:p.Glu141ArgfsTer24
ENST00000531380.1:c.420dup (FZD4) ENSP00000434034.1:p.Glu141ArgfsTer24
ENST00000532234.5:c.*1329dup (PRSS23) ENSP00000436676.1:n.*1329dup
ENST00000533902.2:c.*1051dup (PRSS23) ENSP00000437268.1:n.*1051dup
NM_012193.3:c.420dup (FZD4) NP_036325.2:p.Glu141ArgfsTer24
NR_120591.1:n.2001dup (PRSS23)
NR_120592.1:n.1750dup (PRSS23)
NR_120591.2:n.1699dup (PRSS23)
NR_120592.2:n.1448dup (PRSS23)
NM_012193.4:c.420dup (FZD4) MANE Select NP_036325.2:p.Glu141ArgfsTer24
NR_120591.3:n.1699dup (PRSS23)