Canonical Allele Identifier: CA476144621

Linked Data

MyVariant Identifiers: chr11:g.86663105G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952063G>A , CM000673.2:g.86952063G>A GRCh38
NC_000011.9:g.86663105G>A , CM000673.1:g.86663105G>A GRCh37
NC_000011.8:g.86340753G>A NCBI36
NG_011752.1:g.8329C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.693C>T (FZD4) MANE Select ENSP00000434034.1:p.Phe231=
ENST00000531380.1:c.693C>T (FZD4) ENSP00000434034.1:p.Phe231=
ENST00000532234.5:c.*1056G>A (PRSS23) ENSP00000436676.1:n.*1056G>A
ENST00000533902.2:c.*778G>A (PRSS23) ENSP00000437268.1:n.*778G>A
NM_012193.3:c.693C>T (FZD4) NP_036325.2:p.Phe231=
NR_120591.1:n.1728G>A (PRSS23)
NR_120592.1:n.1477G>A (PRSS23)
NR_120591.2:n.1426G>A (PRSS23)
NR_120592.2:n.1175G>A (PRSS23)
NM_012193.4:c.693C>T (FZD4) MANE Select NP_036325.2:p.Phe231=
NR_120591.3:n.1426G>A (PRSS23)