Canonical Allele Identifier: CA476145151

Linked Data

MyVariant Identifiers: chr11:g.86663402C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952360C>A , CM000673.2:g.86952360C>A GRCh38
NC_000011.9:g.86663402C>A , CM000673.1:g.86663402C>A GRCh37
NC_000011.8:g.86341050C>A NCBI36
NG_011752.1:g.8032G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.396G>T (FZD4) MANE Select ENSP00000434034.1:p.Leu132=
ENST00000531380.1:c.396G>T (FZD4) ENSP00000434034.1:p.Leu132=
ENST00000532234.5:c.*1353C>A (PRSS23) ENSP00000436676.1:n.*1353C>A
ENST00000533902.2:c.*1075C>A (PRSS23) ENSP00000437268.1:n.*1075C>A
NM_012193.3:c.396G>T (FZD4) NP_036325.2:p.Leu132=
NR_120591.1:n.2025C>A (PRSS23)
NR_120592.1:n.1774C>A (PRSS23)
NR_120591.2:n.1723C>A (PRSS23)
NR_120592.2:n.1472C>A (PRSS23)
NM_012193.4:c.396G>T (FZD4) MANE Select NP_036325.2:p.Leu132=
NR_120591.3:n.1723C>A (PRSS23)