Canonical Allele Identifier: CA476144471

Linked Data

MyVariant Identifiers: chr11:g.86662622C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951580C>T , CM000673.2:g.86951580C>T GRCh38
NC_000011.9:g.86662622C>T , CM000673.1:g.86662622C>T GRCh37
NC_000011.8:g.86340270C>T NCBI36
NG_011752.1:g.8812G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.1176G>A (FZD4) MANE Select ENSP00000434034.1:p.Val392=
ENST00000531380.1:c.1176G>A (FZD4) ENSP00000434034.1:p.Val392=
ENST00000531521.1:n.751C>T (PRSS23)
ENST00000532234.5:c.*573C>T (PRSS23) ENSP00000436676.1:n.*573C>T
ENST00000533902.2:c.*295C>T (PRSS23) ENSP00000437268.1:n.*295C>T
NM_012193.3:c.1176G>A (FZD4) NP_036325.2:p.Val392=
NR_120591.1:n.1245C>T (PRSS23)
NR_120592.1:n.994C>T (PRSS23)
NR_120591.2:n.943C>T (PRSS23)
NR_120592.2:n.692C>T (PRSS23)
NM_012193.4:c.1176G>A (FZD4) MANE Select NP_036325.2:p.Val392=
NR_120591.3:n.943C>T (PRSS23)