Canonical Allele Identifier: CA382011553

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951396A>T , CM000673.2:g.86951396A>T GRCh38
NC_000011.9:g.86662438A>T , CM000673.1:g.86662438A>T GRCh37
NC_000011.8:g.86340086A>T NCBI36
NG_011752.1:g.8996T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.1360T>A (FZD4) MANE Select ENSP00000434034.1:p.Cys454Ser
ENST00000528769.5:n.453A>T (PRSS23)
ENST00000531380.1:c.1360T>A (FZD4) ENSP00000434034.1:p.Cys454Ser
ENST00000531521.1:n.567A>T (PRSS23)
ENST00000532234.5:c.*389A>T (PRSS23) ENSP00000436676.1:n.*389A>T
ENST00000533902.2:c.*111A>T (PRSS23) ENSP00000437268.1:n.*111A>T
NM_012193.3:c.1360T>A (FZD4) NP_036325.2:p.Cys454Ser
NR_120591.1:n.1061A>T (PRSS23)
NR_120592.1:n.810A>T (PRSS23)
NR_120591.2:n.759A>T (PRSS23)
NR_120592.2:n.508A>T (PRSS23)
NM_012193.4:c.1360T>A (FZD4) MANE Select NP_036325.2:p.Cys454Ser
NR_120591.3:n.759A>T (PRSS23)