Canonical Allele Identifier: CA2615461017

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86950908G>T , CM000673.2:g.86950908G>T GRCh38
NC_000011.9:g.86661950G>T , CM000673.1:g.86661950G>T GRCh37
NC_000011.8:g.86339598G>T NCBI36
NG_011752.1:g.9484C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.*234C>A (FZD4) MANE Select ENSP00000434034.1:n.*234C>A
ENST00000528769.5:n.273-308G>T (PRSS23)
ENST00000531380.1:c.*234C>A (FZD4) ENSP00000434034.1:n.*234C>A
ENST00000531521.1:n.387-308G>T (PRSS23)
ENST00000532234.5:c.*209-308G>T (PRSS23) ENSP00000436676.1:n.*209-308G>T
ENST00000533902.2:c.207-308G>T (PRSS23) ENSP00000437268.1:n.207-308G>T
NM_012193.3:c.*234C>A (FZD4) NP_036325.2:n.*234C>A
NR_120591.1:n.881-308G>T (PRSS23)
NR_120592.1:n.630-308G>T (PRSS23)
NR_120591.2:n.579-308G>T (PRSS23)
NR_120592.2:n.328-308G>T (PRSS23)
NM_012193.4:c.*234C>A (FZD4) MANE Select NP_036325.2:n.*234C>A
NR_120591.3:n.579-308G>T (PRSS23)