Canonical Allele Identifier: CA1988807771

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951287G= , CM000673.2:g.86951287G= GRCh38
NC_000011.9:g.86662329G= , CM000673.1:g.86662329G= GRCh37
NC_000011.8:g.86339977G= NCBI36
NG_011752.1:g.9105C=

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.1469C= (FZD4) MANE Select ENSP00000434034.1:p.Thr490=
ENST00000528769.5:n.344G= (PRSS23)
ENST00000531380.1:c.1469C= (FZD4) ENSP00000434034.1:p.Thr490=
ENST00000531521.1:n.458G= (PRSS23)
ENST00000532234.5:c.*280G= (PRSS23) ENSP00000436676.1:n.*280G=
ENST00000533902.2:c.*2G= (PRSS23) ENSP00000437268.1:n.*2G=
NM_012193.3:c.1469C= (FZD4) NP_036325.2:p.Thr490=
NR_120591.1:n.952G= (PRSS23)
NR_120592.1:n.701G= (PRSS23)
NR_120591.2:n.650G= (PRSS23)
NR_120592.2:n.399G= (PRSS23)
NM_012193.4:c.1469C= (FZD4) MANE Select NP_036325.2:p.Thr490=
NR_120591.3:n.650G= (PRSS23)