Canonical Allele Identifier: CA476144369

Linked Data

MyVariant Identifiers: chr11:g.86662469C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951427C>A , CM000673.2:g.86951427C>A GRCh38
NC_000011.9:g.86662469C>A , CM000673.1:g.86662469C>A GRCh37
NC_000011.8:g.86340117C>A NCBI36
NG_011752.1:g.8965G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.1329G>T (FZD4) MANE Select ENSP00000434034.1:p.Leu443=
ENST00000531380.1:c.1329G>T (FZD4) ENSP00000434034.1:p.Leu443=
ENST00000531521.1:n.598C>A (PRSS23)
ENST00000532234.5:c.*420C>A (PRSS23) ENSP00000436676.1:n.*420C>A
ENST00000533902.2:c.*142C>A (PRSS23) ENSP00000437268.1:n.*142C>A
NM_012193.3:c.1329G>T (FZD4) NP_036325.2:p.Leu443=
NR_120591.1:n.1092C>A (PRSS23)
NR_120592.1:n.841C>A (PRSS23)
NR_120591.2:n.790C>A (PRSS23)
NR_120592.2:n.539C>A (PRSS23)
NM_012193.4:c.1329G>T (FZD4) MANE Select NP_036325.2:p.Leu443=
NR_120591.3:n.790C>A (PRSS23)