Canonical Allele Identifier: CA2615455664

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86946435G>T , CM000673.2:g.86946435G>T GRCh38
NC_000011.9:g.86657477G>T , CM000673.1:g.86657477G>T GRCh37
NC_000011.8:g.86335125G>T NCBI36
NG_011752.1:g.13957C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.*4707C>A (FZD4) MANE Select ENSP00000434034.1:n.*4707C>A
ENST00000528769.5:n.129-3921G>T (PRSS23)
ENST00000531380.1:c.*4707C>A (FZD4) ENSP00000434034.1:n.*4707C>A
ENST00000531521.1:n.243-3921G>T (PRSS23)
ENST00000532234.5:c.*65-3921G>T (PRSS23) ENSP00000436676.1:n.*65-3921G>T
ENST00000533902.2:c.207-4781G>T (PRSS23) ENSP00000437268.1:n.207-4781G>T
NM_012193.3:c.*4707C>A (FZD4) NP_036325.2:n.*4707C>A
NR_120591.1:n.737-3921G>T (PRSS23)
NR_120592.1:n.630-4781G>T (PRSS23)
NR_120591.2:n.435-3921G>T (PRSS23)
NR_120592.2:n.328-4781G>T (PRSS23)
NM_012193.4:c.*4707C>A (FZD4) MANE Select NP_036325.2:n.*4707C>A
NR_120591.3:n.435-3921G>T (PRSS23)