Canonical Allele Identifier: CA382016653

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952344C>T , CM000673.2:g.86952344C>T GRCh38
NC_000011.9:g.86663386C>T , CM000673.1:g.86663386C>T GRCh37
NC_000011.8:g.86341034C>T NCBI36
NG_011752.1:g.8048G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.412G>A (FZD4) MANE Select ENSP00000434034.1:p.Ala138Thr
ENST00000531380.1:c.412G>A (FZD4) ENSP00000434034.1:p.Ala138Thr
ENST00000532234.5:c.*1337C>T (PRSS23) ENSP00000436676.1:n.*1337C>T
ENST00000533902.2:c.*1059C>T (PRSS23) ENSP00000437268.1:n.*1059C>T
NM_012193.3:c.412G>A (FZD4) NP_036325.2:p.Ala138Thr
NR_120591.1:n.2009C>T (PRSS23)
NR_120592.1:n.1758C>T (PRSS23)
NR_120591.2:n.1707C>T (PRSS23)
NR_120592.2:n.1456C>T (PRSS23)
NM_012193.4:c.412G>A (FZD4) MANE Select NP_036325.2:p.Ala138Thr
NR_120591.3:n.1707C>T (PRSS23)