Canonical Allele Identifier: CA382010971

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951228T>C , CM000673.2:g.86951228T>C GRCh38
NC_000011.9:g.86662270T>C , CM000673.1:g.86662270T>C GRCh37
NC_000011.8:g.86339918T>C NCBI36
NG_011752.1:g.9164A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.1528A>G (FZD4) MANE Select ENSP00000434034.1:p.Arg510Gly
ENST00000528769.5:n.285T>C (PRSS23)
ENST00000531380.1:c.1528A>G (FZD4) ENSP00000434034.1:p.Arg510Gly
ENST00000531521.1:n.399T>C (PRSS23)
ENST00000532234.5:c.*221T>C (PRSS23) ENSP00000436676.1:n.*221T>C
ENST00000533902.2:c.219T>C (PRSS23) ENSP00000437268.1:p.Ser73=
NM_012193.3:c.1528A>G (FZD4) NP_036325.2:p.Arg510Gly
NR_120591.1:n.893T>C (PRSS23)
NR_120592.1:n.642T>C (PRSS23)
NR_120591.2:n.591T>C (PRSS23)
NR_120592.2:n.340T>C (PRSS23)
NM_012193.4:c.1528A>G (FZD4) MANE Select NP_036325.2:p.Arg510Gly
NR_120591.3:n.591T>C (PRSS23)