Canonical Allele Identifier: CA3182875327
Community Standard Title: NM_012193.4(FZD4):c.288C= (p.Phe96=)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952468G= , CM000673.2:g.86952468G= GRCh38
NC_000011.9:g.86663510G= , CM000673.1:g.86663510G= GRCh37
NC_000011.8:g.86341158G= NCBI36
NG_011752.1:g.7924C=

Transcript Alleles

HGVS Amino-acid Change
NM_012193.4:c.288C= (FZD4) MANE Select NP_036325.2:p.Phe96=
ENST00000531380.2:c.288C= (FZD4) MANE Select ENSP00000434034.1:p.Phe96=
NM_012193.3:c.288C= (FZD4) NP_036325.2:p.Phe96=
NR_120591.1:n.2133G= (PRSS23)
NR_120591.2:n.1831G= (PRSS23)
NR_120591.3:n.1831G= (PRSS23)
NR_120592.1:n.1882G= (PRSS23)
NR_120592.2:n.1580G= (PRSS23)
ENST00000531380.1:c.288C= (FZD4) ENSP00000434034.1:p.Phe96=
ENST00000532234.5:c.*1461G= (PRSS23) ENSP00000436676.1:n.*1461G=
ENST00000533902.2:c.*1183G= (PRSS23) ENSP00000437268.1:n.*1183G=