Canonical Allele Identifier: CA382011648

Linked Data

dbSNP Id: rs1378438998

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951416G>A , CM000673.2:g.86951416G>A GRCh38
NC_000011.9:g.86662458G>A , CM000673.1:g.86662458G>A GRCh37
NC_000011.8:g.86340106G>A NCBI36
NG_011752.1:g.8976C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.1340C>T (FZD4) MANE Select ENSP00000434034.1:p.Pro447Leu
ENST00000531380.1:c.1340C>T (FZD4) ENSP00000434034.1:p.Pro447Leu
ENST00000531521.1:n.587G>A (PRSS23)
ENST00000532234.5:c.*409G>A (PRSS23) ENSP00000436676.1:n.*409G>A
ENST00000533902.2:c.*131G>A (PRSS23) ENSP00000437268.1:n.*131G>A
NM_012193.3:c.1340C>T (FZD4) NP_036325.2:p.Pro447Leu
NR_120591.1:n.1081G>A (PRSS23)
NR_120592.1:n.830G>A (PRSS23)
NR_120591.2:n.779G>A (PRSS23)
NR_120592.2:n.528G>A (PRSS23)
NM_012193.4:c.1340C>T (FZD4) MANE Select NP_036325.2:p.Pro447Leu
NR_120591.3:n.779G>A (PRSS23)