Canonical Allele Identifier: CA476145106

Linked Data

MyVariant Identifiers: chr11:g.86663297C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952255C>T , CM000673.2:g.86952255C>T GRCh38
NC_000011.9:g.86663297C>T , CM000673.1:g.86663297C>T GRCh37
NC_000011.8:g.86340945C>T NCBI36
NG_011752.1:g.8137G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.501G>A (FZD4) MANE Select ENSP00000434034.1:p.Val167=
ENST00000531380.1:c.501G>A (FZD4) ENSP00000434034.1:p.Val167=
ENST00000532234.5:c.*1248C>T (PRSS23) ENSP00000436676.1:n.*1248C>T
ENST00000533902.2:c.*970C>T (PRSS23) ENSP00000437268.1:n.*970C>T
NM_012193.3:c.501G>A (FZD4) NP_036325.2:p.Val167=
NR_120591.1:n.1920C>T (PRSS23)
NR_120592.1:n.1669C>T (PRSS23)
NR_120591.2:n.1618C>T (PRSS23)
NR_120592.2:n.1367C>T (PRSS23)
NM_012193.4:c.501G>A (FZD4) MANE Select NP_036325.2:p.Val167=
NR_120591.3:n.1618C>T (PRSS23)