Canonical Allele Identifier: CA1988808088

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951506C= , CM000673.2:g.86951506C= GRCh38
NC_000011.9:g.86662548C= , CM000673.1:g.86662548C= GRCh37
NC_000011.8:g.86340196C= NCBI36
NG_011752.1:g.8886G=

Transcript Alleles

HGVS Amino-acid Change
NM_012193.4:c.1250G= (FZD4) MANE Select NP_036325.2:p.Arg417=
ENST00000531380.2:c.1250G= (FZD4) MANE Select ENSP00000434034.1:p.Arg417=
NM_012193.3:c.1250G= (FZD4) NP_036325.2:p.Arg417=
NR_120591.1:n.1171C= (PRSS23)
NR_120591.2:n.869C= (PRSS23)
NR_120591.3:n.869C= (PRSS23)
NR_120592.1:n.920C= (PRSS23)
NR_120592.2:n.618C= (PRSS23)
ENST00000531380.1:c.1250G= (FZD4) ENSP00000434034.1:p.Arg417=
ENST00000531521.1:n.677C= (PRSS23)
ENST00000532234.5:c.*499C= (PRSS23) ENSP00000436676.1:n.*499C=
ENST00000533902.2:c.*221C= (PRSS23) ENSP00000437268.1:n.*221C=