Canonical Allele Identifier: CA476144493

Linked Data

MyVariant Identifiers: chr11:g.86662658T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951616T>G , CM000673.2:g.86951616T>G GRCh38
NC_000011.9:g.86662658T>G , CM000673.1:g.86662658T>G GRCh37
NC_000011.8:g.86340306T>G NCBI36
NG_011752.1:g.8776A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.1140A>C (FZD4) MANE Select ENSP00000434034.1:p.Gly380=
ENST00000531380.1:c.1140A>C (FZD4) ENSP00000434034.1:p.Gly380=
ENST00000531521.1:n.787T>G (PRSS23)
ENST00000532234.5:c.*609T>G (PRSS23) ENSP00000436676.1:n.*609T>G
ENST00000533902.2:c.*331T>G (PRSS23) ENSP00000437268.1:n.*331T>G
NM_012193.3:c.1140A>C (FZD4) NP_036325.2:p.Gly380=
NR_120591.1:n.1281T>G (PRSS23)
NR_120592.1:n.1030T>G (PRSS23)
NR_120591.2:n.979T>G (PRSS23)
NR_120592.2:n.728T>G (PRSS23)
NM_012193.4:c.1140A>C (FZD4) MANE Select NP_036325.2:p.Gly380=
NR_120591.3:n.979T>G (PRSS23)