Canonical Allele Identifier: CA382011569

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951399C>T , CM000673.2:g.86951399C>T GRCh38
NC_000011.9:g.86662441C>T , CM000673.1:g.86662441C>T GRCh37
NC_000011.8:g.86340089C>T NCBI36
NG_011752.1:g.8993G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.1357G>A (FZD4) MANE Select ENSP00000434034.1:p.Ala453Thr
ENST00000528769.5:n.456C>T (PRSS23)
ENST00000531380.1:c.1357G>A (FZD4) ENSP00000434034.1:p.Ala453Thr
ENST00000531521.1:n.570C>T (PRSS23)
ENST00000532234.5:c.*392C>T (PRSS23) ENSP00000436676.1:n.*392C>T
ENST00000533902.2:c.*114C>T (PRSS23) ENSP00000437268.1:n.*114C>T
NM_012193.3:c.1357G>A (FZD4) NP_036325.2:p.Ala453Thr
NR_120591.1:n.1064C>T (PRSS23)
NR_120592.1:n.813C>T (PRSS23)
NR_120591.2:n.762C>T (PRSS23)
NR_120592.2:n.511C>T (PRSS23)
NM_012193.4:c.1357G>A (FZD4) MANE Select NP_036325.2:p.Ala453Thr
NR_120591.3:n.762C>T (PRSS23)