Canonical Allele Identifier: CA1988808022

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951442C= , CM000673.2:g.86951442C= GRCh38
NC_000011.9:g.86662484C= , CM000673.1:g.86662484C= GRCh37
NC_000011.8:g.86340132C= NCBI36
NG_011752.1:g.8950G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.1314G= (FZD4) MANE Select ENSP00000434034.1:p.Gly438=
ENST00000531380.1:c.1314G= (FZD4) ENSP00000434034.1:p.Gly438=
ENST00000531521.1:n.613C= (PRSS23)
ENST00000532234.5:c.*435C= (PRSS23) ENSP00000436676.1:n.*435C=
ENST00000533902.2:c.*157C= (PRSS23) ENSP00000437268.1:n.*157C=
NM_012193.3:c.1314G= (FZD4) NP_036325.2:p.Gly438=
NR_120591.1:n.1107C= (PRSS23)
NR_120592.1:n.856C= (PRSS23)
NR_120591.2:n.805C= (PRSS23)
NR_120592.2:n.554C= (PRSS23)
NM_012193.4:c.1314G= (FZD4) MANE Select NP_036325.2:p.Gly438=
NR_120591.3:n.805C= (PRSS23)