Canonical Allele Identifier: CA382016865

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952371C>T , CM000673.2:g.86952371C>T GRCh38
NC_000011.9:g.86663413C>T , CM000673.1:g.86663413C>T GRCh37
NC_000011.8:g.86341061C>T NCBI36
NG_011752.1:g.8021G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.385G>A (FZD4) MANE Select ENSP00000434034.1:p.Glu129Lys
ENST00000531380.1:c.385G>A (FZD4) ENSP00000434034.1:p.Glu129Lys
ENST00000532234.5:c.*1364C>T (PRSS23) ENSP00000436676.1:n.*1364C>T
ENST00000533902.2:c.*1086C>T (PRSS23) ENSP00000437268.1:n.*1086C>T
NM_012193.3:c.385G>A (FZD4) NP_036325.2:p.Glu129Lys
NR_120591.1:n.2036C>T (PRSS23)
NR_120592.1:n.1785C>T (PRSS23)
NR_120591.2:n.1734C>T (PRSS23)
NR_120592.2:n.1483C>T (PRSS23)
NM_012193.4:c.385G>A (FZD4) MANE Select NP_036325.2:p.Glu129Lys
NR_120591.3:n.1734C>T (PRSS23)