Canonical Allele Identifier: CA382014502

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951993T>A , CM000673.2:g.86951993T>A GRCh38
NC_000011.9:g.86663035T>A , CM000673.1:g.86663035T>A GRCh37
NC_000011.8:g.86340683T>A NCBI36
NG_011752.1:g.8399A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.763A>T (FZD4) MANE Select ENSP00000434034.1:p.Ile255Phe
ENST00000531380.1:c.763A>T (FZD4) ENSP00000434034.1:p.Ile255Phe
ENST00000532234.5:c.*986T>A (PRSS23) ENSP00000436676.1:n.*986T>A
ENST00000533902.2:c.*708T>A (PRSS23) ENSP00000437268.1:n.*708T>A
NM_012193.3:c.763A>T (FZD4) NP_036325.2:p.Ile255Phe
NR_120591.1:n.1658T>A (PRSS23)
NR_120592.1:n.1407T>A (PRSS23)
NR_120591.2:n.1356T>A (PRSS23)
NR_120592.2:n.1105T>A (PRSS23)
NM_012193.4:c.763A>T (FZD4) MANE Select NP_036325.2:p.Ile255Phe
NR_120591.3:n.1356T>A (PRSS23)