Canonical Allele Identifier: CA6218363

Linked Data

dbSNP Id: rs754959108

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951582C>T , CM000673.2:g.86951582C>T GRCh38
NC_000011.9:g.86662624C>T , CM000673.1:g.86662624C>T GRCh37
NC_000011.8:g.86340272C>T NCBI36
NG_011752.1:g.8810G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.1174G>A (FZD4) MANE Select ENSP00000434034.1:p.Val392Met
ENST00000531380.1:c.1174G>A (FZD4) ENSP00000434034.1:p.Val392Met
ENST00000531521.1:n.753C>T (PRSS23)
ENST00000532234.5:c.*575C>T (PRSS23) ENSP00000436676.1:n.*575C>T
ENST00000533902.2:c.*297C>T (PRSS23) ENSP00000437268.1:n.*297C>T
NM_012193.3:c.1174G>A (FZD4) NP_036325.2:p.Val392Met
NR_120591.1:n.1247C>T (PRSS23)
NR_120592.1:n.996C>T (PRSS23)
NR_120591.2:n.945C>T (PRSS23)
NR_120592.2:n.694C>T (PRSS23)
NM_012193.4:c.1174G>A (FZD4) MANE Select NP_036325.2:p.Val392Met
NR_120591.3:n.945C>T (PRSS23)