Canonical Allele Identifier: CA476144480

Linked Data

dbSNP Id: rs2135040499
MyVariant Identifiers: chr11:g.86662637G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951595G>A , CM000673.2:g.86951595G>A GRCh38
NC_000011.9:g.86662637G>A , CM000673.1:g.86662637G>A GRCh37
NC_000011.8:g.86340285G>A NCBI36
NG_011752.1:g.8797C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.1161C>T (FZD4) MANE Select ENSP00000434034.1:p.Leu387=
ENST00000531380.1:c.1161C>T (FZD4) ENSP00000434034.1:p.Leu387=
ENST00000531521.1:n.766G>A (PRSS23)
ENST00000532234.5:c.*588G>A (PRSS23) ENSP00000436676.1:n.*588G>A
ENST00000533902.2:c.*310G>A (PRSS23) ENSP00000437268.1:n.*310G>A
NM_012193.3:c.1161C>T (FZD4) NP_036325.2:p.Leu387=
NR_120591.1:n.1260G>A (PRSS23)
NR_120592.1:n.1009G>A (PRSS23)
NR_120591.2:n.958G>A (PRSS23)
NR_120592.2:n.707G>A (PRSS23)
NM_012193.4:c.1161C>T (FZD4) MANE Select NP_036325.2:p.Leu387=
NR_120591.3:n.958G>A (PRSS23)