Canonical Allele Identifier: CA382017034

Linked Data

dbSNP Id: rs1949301956

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952396C>A , CM000673.2:g.86952396C>A GRCh38
NC_000011.9:g.86663438C>A , CM000673.1:g.86663438C>A GRCh37
NC_000011.8:g.86341086C>A NCBI36
NG_011752.1:g.7996G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.360G>T (FZD4) MANE Select ENSP00000434034.1:p.Met120Ile
ENST00000531380.1:c.360G>T (FZD4) ENSP00000434034.1:p.Met120Ile
ENST00000532234.5:c.*1389C>A (PRSS23) ENSP00000436676.1:n.*1389C>A
ENST00000533902.2:c.*1111C>A (PRSS23) ENSP00000437268.1:n.*1111C>A
NM_012193.3:c.360G>T (FZD4) NP_036325.2:p.Met120Ile
NR_120591.1:n.2061C>A (PRSS23)
NR_120592.1:n.1810C>A (PRSS23)
NR_120591.2:n.1759C>A (PRSS23)
NR_120592.2:n.1508C>A (PRSS23)
NM_012193.4:c.360G>T (FZD4) MANE Select NP_036325.2:p.Met120Ile
NR_120591.3:n.1759C>A (PRSS23)