Canonical Allele Identifier: CA1988809043

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952196T= , CM000673.2:g.86952196T= GRCh38
NC_000011.9:g.86663238T= , CM000673.1:g.86663238T= GRCh37
NC_000011.8:g.86340886T= NCBI36
NG_011752.1:g.8196A=

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.560A= (FZD4) MANE Select ENSP00000434034.1:p.Asn187=
ENST00000531380.1:c.560A= (FZD4) ENSP00000434034.1:p.Asn187=
ENST00000532234.5:c.*1189T= (PRSS23) ENSP00000436676.1:n.*1189T=
ENST00000533902.2:c.*911T= (PRSS23) ENSP00000437268.1:n.*911T=
NM_012193.3:c.560A= (FZD4) NP_036325.2:p.Asn187=
NR_120591.1:n.1861T= (PRSS23)
NR_120592.1:n.1610T= (PRSS23)
NR_120591.2:n.1559T= (PRSS23)
NR_120592.2:n.1308T= (PRSS23)
NM_012193.4:c.560A= (FZD4) MANE Select NP_036325.2:p.Asn187=
NR_120591.3:n.1559T= (PRSS23)