Canonical Allele Identifier: CA1988808844

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952076G= , CM000673.2:g.86952076G= GRCh38
NC_000011.9:g.86663118G= , CM000673.1:g.86663118G= GRCh37
NC_000011.8:g.86340766G= NCBI36
NG_011752.1:g.8316C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.680C= (FZD4) MANE Select ENSP00000434034.1:p.Ala227=
ENST00000531380.1:c.680C= (FZD4) ENSP00000434034.1:p.Ala227=
ENST00000532234.5:c.*1069G= (PRSS23) ENSP00000436676.1:n.*1069G=
ENST00000533902.2:c.*791G= (PRSS23) ENSP00000437268.1:n.*791G=
NM_012193.3:c.680C= (FZD4) NP_036325.2:p.Ala227=
NR_120591.1:n.1741G= (PRSS23)
NR_120592.1:n.1490G= (PRSS23)
NR_120591.2:n.1439G= (PRSS23)
NR_120592.2:n.1188G= (PRSS23)
NM_012193.4:c.680C= (FZD4) MANE Select NP_036325.2:p.Ala227=
NR_120591.3:n.1439G= (PRSS23)