Canonical Allele Identifier: CA382015974

Linked Data

COSMIC: COSM344078

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952263C>T , CM000673.2:g.86952263C>T GRCh38
NC_000011.9:g.86663305C>T , CM000673.1:g.86663305C>T GRCh37
NC_000011.8:g.86340953C>T NCBI36
NG_011752.1:g.8129G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.493G>A (FZD4) MANE Select ENSP00000434034.1:p.Glu165Lys
ENST00000531380.1:c.493G>A (FZD4) ENSP00000434034.1:p.Glu165Lys
ENST00000532234.5:c.*1256C>T (PRSS23) ENSP00000436676.1:n.*1256C>T
ENST00000533902.2:c.*978C>T (PRSS23) ENSP00000437268.1:n.*978C>T
NM_012193.3:c.493G>A (FZD4) NP_036325.2:p.Glu165Lys
NR_120591.1:n.1928C>T (PRSS23)
NR_120592.1:n.1677C>T (PRSS23)
NR_120591.2:n.1626C>T (PRSS23)
NR_120592.2:n.1375C>T (PRSS23)
NM_012193.4:c.493G>A (FZD4) MANE Select NP_036325.2:p.Glu165Lys
NR_120591.3:n.1626C>T (PRSS23)