Canonical Allele Identifier: CA382012126

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951489C>T , CM000673.2:g.86951489C>T GRCh38
NC_000011.9:g.86662531C>T , CM000673.1:g.86662531C>T GRCh37
NC_000011.8:g.86340179C>T NCBI36
NG_011752.1:g.8903G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.1267G>A (FZD4) MANE Select ENSP00000434034.1:p.Asp423Asn
ENST00000531380.1:c.1267G>A (FZD4) ENSP00000434034.1:p.Asp423Asn
ENST00000531521.1:n.660C>T (PRSS23)
ENST00000532234.5:c.*482C>T (PRSS23) ENSP00000436676.1:n.*482C>T
ENST00000533902.2:c.*204C>T (PRSS23) ENSP00000437268.1:n.*204C>T
NM_012193.3:c.1267G>A (FZD4) NP_036325.2:p.Asp423Asn
NR_120591.1:n.1154C>T (PRSS23)
NR_120592.1:n.903C>T (PRSS23)
NR_120591.2:n.852C>T (PRSS23)
NR_120592.2:n.601C>T (PRSS23)
NM_012193.4:c.1267G>A (FZD4) MANE Select NP_036325.2:p.Asp423Asn
NR_120591.3:n.852C>T (PRSS23)