Canonical Allele Identifier: CA476144378

Linked Data

dbSNP Id: rs1590943260
MyVariant Identifiers: chr11:g.86662481C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951439C>T , CM000673.2:g.86951439C>T GRCh38
NC_000011.9:g.86662481C>T , CM000673.1:g.86662481C>T GRCh37
NC_000011.8:g.86340129C>T NCBI36
NG_011752.1:g.8953G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.1317G>A (FZD4) MANE Select ENSP00000434034.1:p.Val439=
ENST00000531380.1:c.1317G>A (FZD4) ENSP00000434034.1:p.Val439=
ENST00000531521.1:n.610C>T (PRSS23)
ENST00000532234.5:c.*432C>T (PRSS23) ENSP00000436676.1:n.*432C>T
ENST00000533902.2:c.*154C>T (PRSS23) ENSP00000437268.1:n.*154C>T
NM_012193.3:c.1317G>A (FZD4) NP_036325.2:p.Val439=
NR_120591.1:n.1104C>T (PRSS23)
NR_120592.1:n.853C>T (PRSS23)
NR_120591.2:n.802C>T (PRSS23)
NR_120592.2:n.551C>T (PRSS23)
NM_012193.4:c.1317G>A (FZD4) MANE Select NP_036325.2:p.Val439=
NR_120591.3:n.802C>T (PRSS23)