Canonical Allele Identifier: CA225381703

Linked Data

dbSNP Id: rs80358285

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952442A>G , CM000673.2:g.86952442A>G GRCh38
NC_000011.9:g.86663484A>G , CM000673.1:g.86663484A>G GRCh37
NC_000011.8:g.86341132A>G NCBI36
NG_011752.1:g.7950T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.314T>C (FZD4) MANE Select ENSP00000434034.1:p.Met105Thr
ENST00000531380.1:c.314T>C (FZD4) ENSP00000434034.1:p.Met105Thr
ENST00000532234.5:c.*1435A>G (PRSS23) ENSP00000436676.1:n.*1435A>G
ENST00000533902.2:c.*1157A>G (PRSS23) ENSP00000437268.1:n.*1157A>G
NM_012193.3:c.314T>C (FZD4) NP_036325.2:p.Met105Thr
NR_120591.1:n.2107A>G (PRSS23)
NR_120592.1:n.1856A>G (PRSS23)
NR_120591.2:n.1805A>G (PRSS23)
NR_120592.2:n.1554A>G (PRSS23)
NM_012193.4:c.314T>C (FZD4) MANE Select NP_036325.2:p.Met105Thr
NR_120591.3:n.1805A>G (PRSS23)