Canonical Allele Identifier: CA476144357

Linked Data

dbSNP Id: rs1157906125

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951412T>C , CM000673.2:g.86951412T>C GRCh38
NC_000011.9:g.86662454T>C , CM000673.1:g.86662454T>C GRCh37
NC_000011.8:g.86340102T>C NCBI36
NG_011752.1:g.8980A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.1344A>G (FZD4) MANE Select ENSP00000434034.1:p.Ala448=
ENST00000531380.1:c.1344A>G (FZD4) ENSP00000434034.1:p.Ala448=
ENST00000531521.1:n.583T>C (PRSS23)
ENST00000532234.5:c.*405T>C (PRSS23) ENSP00000436676.1:n.*405T>C
ENST00000533902.2:c.*127T>C (PRSS23) ENSP00000437268.1:n.*127T>C
NM_012193.3:c.1344A>G (FZD4) NP_036325.2:p.Ala448=
NR_120591.1:n.1077T>C (PRSS23)
NR_120592.1:n.826T>C (PRSS23)
NR_120591.2:n.775T>C (PRSS23)
NR_120592.2:n.524T>C (PRSS23)
NM_012193.4:c.1344A>G (FZD4) MANE Select NP_036325.2:p.Ala448=
NR_120591.3:n.775T>C (PRSS23)