Canonical Allele Identifier: CA1988809242

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952354T= , CM000673.2:g.86952354T= GRCh38
NC_000011.9:g.86663396T= , CM000673.1:g.86663396T= GRCh37
NC_000011.8:g.86341044T= NCBI36
NG_011752.1:g.8038A=

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.402A= (FZD4) MANE Select ENSP00000434034.1:p.Glu134=
ENST00000531380.1:c.402A= (FZD4) ENSP00000434034.1:p.Glu134=
ENST00000532234.5:c.*1347T= (PRSS23) ENSP00000436676.1:n.*1347T=
ENST00000533902.2:c.*1069T= (PRSS23) ENSP00000437268.1:n.*1069T=
NM_012193.3:c.402A= (FZD4) NP_036325.2:p.Glu134=
NR_120591.1:n.2019T= (PRSS23)
NR_120592.1:n.1768T= (PRSS23)
NR_120591.2:n.1717T= (PRSS23)
NR_120592.2:n.1466T= (PRSS23)
NM_012193.4:c.402A= (FZD4) MANE Select NP_036325.2:p.Glu134=
NR_120591.3:n.1717T= (PRSS23)