Canonical Allele Identifier: CA382011119

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951282C>A , CM000673.2:g.86951282C>A GRCh38
NC_000011.9:g.86662324C>A , CM000673.1:g.86662324C>A GRCh37
NC_000011.8:g.86339972C>A NCBI36
NG_011752.1:g.9110G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.1474G>T (FZD4) MANE Select ENSP00000434034.1:p.Gly492Cys
ENST00000528769.5:n.339C>A (PRSS23)
ENST00000531380.1:c.1474G>T (FZD4) ENSP00000434034.1:p.Gly492Cys
ENST00000531521.1:n.453C>A (PRSS23)
ENST00000532234.5:c.*275C>A (PRSS23) ENSP00000436676.1:n.*275C>A
ENST00000533902.2:c.273C>A (PRSS23) ENSP00000437268.1:p.Ala91=
NM_012193.3:c.1474G>T (FZD4) NP_036325.2:p.Gly492Cys
NR_120591.1:n.947C>A (PRSS23)
NR_120592.1:n.696C>A (PRSS23)
NR_120591.2:n.645C>A (PRSS23)
NR_120592.2:n.394C>A (PRSS23)
NM_012193.4:c.1474G>T (FZD4) MANE Select NP_036325.2:p.Gly492Cys
NR_120591.3:n.645C>A (PRSS23)