Canonical Allele Identifier: CA476144248

Linked Data

MyVariant Identifiers: chr11:g.86662193A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951151A>G , CM000673.2:g.86951151A>G GRCh38
NC_000011.9:g.86662193A>G , CM000673.1:g.86662193A>G GRCh37
NC_000011.8:g.86339841A>G NCBI36
NG_011752.1:g.9241T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.1605T>C (FZD4) MANE Select ENSP00000434034.1:p.Thr535=
ENST00000528769.5:n.273-65A>G (PRSS23)
ENST00000531380.1:c.1605T>C (FZD4) ENSP00000434034.1:p.Thr535=
ENST00000531521.1:n.387-65A>G (PRSS23)
ENST00000532234.5:c.*209-65A>G (PRSS23) ENSP00000436676.1:n.*209-65A>G
ENST00000533902.2:c.207-65A>G (PRSS23) ENSP00000437268.1:n.207-65A>G
NM_012193.3:c.1605T>C (FZD4) NP_036325.2:p.Thr535=
NR_120591.1:n.881-65A>G (PRSS23)
NR_120592.1:n.630-65A>G (PRSS23)
NR_120591.2:n.579-65A>G (PRSS23)
NR_120592.2:n.328-65A>G (PRSS23)
NM_012193.4:c.1605T>C (FZD4) MANE Select NP_036325.2:p.Thr535=
NR_120591.3:n.579-65A>G (PRSS23)