Canonical Allele Identifier: CA382010862

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951180A>C , CM000673.2:g.86951180A>C GRCh38
NC_000011.9:g.86662222A>C , CM000673.1:g.86662222A>C GRCh37
NC_000011.8:g.86339870A>C NCBI36
NG_011752.1:g.9212T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.1576T>G (FZD4) MANE Select ENSP00000434034.1:p.Trp526Gly
ENST00000528769.5:n.273-36A>C (PRSS23)
ENST00000531380.1:c.1576T>G (FZD4) ENSP00000434034.1:p.Trp526Gly
ENST00000531521.1:n.387-36A>C (PRSS23)
ENST00000532234.5:c.*209-36A>C (PRSS23) ENSP00000436676.1:n.*209-36A>C
ENST00000533902.2:c.207-36A>C (PRSS23) ENSP00000437268.1:n.207-36A>C
NM_012193.3:c.1576T>G (FZD4) NP_036325.2:p.Trp526Gly
NR_120591.1:n.881-36A>C (PRSS23)
NR_120592.1:n.630-36A>C (PRSS23)
NR_120591.2:n.579-36A>C (PRSS23)
NR_120592.2:n.328-36A>C (PRSS23)
NM_012193.4:c.1576T>G (FZD4) MANE Select NP_036325.2:p.Trp526Gly
NR_120591.3:n.579-36A>C (PRSS23)