Canonical Allele Identifier: CA382016830

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952364A>T , CM000673.2:g.86952364A>T GRCh38
NC_000011.9:g.86663406A>T , CM000673.1:g.86663406A>T GRCh37
NC_000011.8:g.86341054A>T NCBI36
NG_011752.1:g.8028T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.392T>A (FZD4) MANE Select ENSP00000434034.1:p.Val131Asp
ENST00000531380.1:c.392T>A (FZD4) ENSP00000434034.1:p.Val131Asp
ENST00000532234.5:c.*1357A>T (PRSS23) ENSP00000436676.1:n.*1357A>T
ENST00000533902.2:c.*1079A>T (PRSS23) ENSP00000437268.1:n.*1079A>T
NM_012193.3:c.392T>A (FZD4) NP_036325.2:p.Val131Asp
NR_120591.1:n.2029A>T (PRSS23)
NR_120592.1:n.1778A>T (PRSS23)
NR_120591.2:n.1727A>T (PRSS23)
NR_120592.2:n.1476A>T (PRSS23)
NM_012193.4:c.392T>A (FZD4) MANE Select NP_036325.2:p.Val131Asp
NR_120591.3:n.1727A>T (PRSS23)