Canonical Allele Identifier: CA476144456

Linked Data

MyVariant Identifiers: chr11:g.86662601C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951559C>T , CM000673.2:g.86951559C>T GRCh38
NC_000011.9:g.86662601C>T , CM000673.1:g.86662601C>T GRCh37
NC_000011.8:g.86340249C>T NCBI36
NG_011752.1:g.8833G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.1197G>A (FZD4) MANE Select ENSP00000434034.1:p.Leu399=
ENST00000531380.1:c.1197G>A (FZD4) ENSP00000434034.1:p.Leu399=
ENST00000531521.1:n.730C>T (PRSS23)
ENST00000532234.5:c.*552C>T (PRSS23) ENSP00000436676.1:n.*552C>T
ENST00000533902.2:c.*274C>T (PRSS23) ENSP00000437268.1:n.*274C>T
NM_012193.3:c.1197G>A (FZD4) NP_036325.2:p.Leu399=
NR_120591.1:n.1224C>T (PRSS23)
NR_120592.1:n.973C>T (PRSS23)
NR_120591.2:n.922C>T (PRSS23)
NR_120592.2:n.671C>T (PRSS23)
NM_012193.4:c.1197G>A (FZD4) MANE Select NP_036325.2:p.Leu399=
NR_120591.3:n.922C>T (PRSS23)