Canonical Allele Identifier: CA2615461275

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951063T>C , CM000673.2:g.86951063T>C GRCh38
NC_000011.9:g.86662105T>C , CM000673.1:g.86662105T>C GRCh37
NC_000011.8:g.86339753T>C NCBI36
NG_011752.1:g.9329A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.*79A>G (FZD4) MANE Select ENSP00000434034.1:n.*79A>G
ENST00000528769.5:n.273-153T>C (PRSS23)
ENST00000531380.1:c.*79A>G (FZD4) ENSP00000434034.1:n.*79A>G
ENST00000531521.1:n.387-153T>C (PRSS23)
ENST00000532234.5:c.*209-153T>C (PRSS23) ENSP00000436676.1:n.*209-153T>C
ENST00000533902.2:c.207-153T>C (PRSS23) ENSP00000437268.1:n.207-153T>C
NM_012193.3:c.*79A>G (FZD4) NP_036325.2:n.*79A>G
NR_120591.1:n.881-153T>C (PRSS23)
NR_120592.1:n.630-153T>C (PRSS23)
NR_120591.2:n.579-153T>C (PRSS23)
NR_120592.2:n.328-153T>C (PRSS23)
NM_012193.4:c.*79A>G (FZD4) MANE Select NP_036325.2:n.*79A>G
NR_120591.3:n.579-153T>C (PRSS23)