Canonical Allele Identifier: CA382011089

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951272A>G , CM000673.2:g.86951272A>G GRCh38
NC_000011.9:g.86662314A>G , CM000673.1:g.86662314A>G GRCh37
NC_000011.8:g.86339962A>G NCBI36
NG_011752.1:g.9120T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.1484T>C (FZD4) MANE Select ENSP00000434034.1:p.Ile495Thr
ENST00000528769.5:n.329A>G (PRSS23)
ENST00000531380.1:c.1484T>C (FZD4) ENSP00000434034.1:p.Ile495Thr
ENST00000531521.1:n.443A>G (PRSS23)
ENST00000532234.5:c.*265A>G (PRSS23) ENSP00000436676.1:n.*265A>G
ENST00000533902.2:c.263A>G (PRSS23) ENSP00000437268.1:p.Asn88Ser
NM_012193.3:c.1484T>C (FZD4) NP_036325.2:p.Ile495Thr
NR_120591.1:n.937A>G (PRSS23)
NR_120592.1:n.686A>G (PRSS23)
NR_120591.2:n.635A>G (PRSS23)
NR_120592.2:n.384A>G (PRSS23)
NM_012193.4:c.1484T>C (FZD4) MANE Select NP_036325.2:p.Ile495Thr
NR_120591.3:n.635A>G (PRSS23)