Canonical Allele Identifier: CA225380610

Linked Data

dbSNP Id: rs80358297

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951423T>G , CM000673.2:g.86951423T>G GRCh38
NC_000011.9:g.86662465T>G , CM000673.1:g.86662465T>G GRCh37
NC_000011.8:g.86340113T>G NCBI36
NG_011752.1:g.8969A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.1333A>C (FZD4) MANE Select ENSP00000434034.1:p.Thr445Pro
ENST00000531380.1:c.1333A>C (FZD4) ENSP00000434034.1:p.Thr445Pro
ENST00000531521.1:n.594T>G (PRSS23)
ENST00000532234.5:c.*416T>G (PRSS23) ENSP00000436676.1:n.*416T>G
ENST00000533902.2:c.*138T>G (PRSS23) ENSP00000437268.1:n.*138T>G
NM_012193.3:c.1333A>C (FZD4) NP_036325.2:p.Thr445Pro
NR_120591.1:n.1088T>G (PRSS23)
NR_120592.1:n.837T>G (PRSS23)
NR_120591.2:n.786T>G (PRSS23)
NR_120592.2:n.535T>G (PRSS23)
NM_012193.4:c.1333A>C (FZD4) MANE Select NP_036325.2:p.Thr445Pro
NR_120591.3:n.786T>G (PRSS23)