Canonical Allele Identifier: CA1988802576

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86946485T= , CM000673.2:g.86946485T= GRCh38
NC_000011.9:g.86657527T= , CM000673.1:g.86657527T= GRCh37
NC_000011.8:g.86335175T= NCBI36
NG_011752.1:g.13907A=

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.*4657A= (FZD4) MANE Select ENSP00000434034.1:n.*4657A=
ENST00000528769.5:n.129-3871T= (PRSS23)
ENST00000531380.1:c.*4657A= (FZD4) ENSP00000434034.1:n.*4657A=
ENST00000531521.1:n.243-3871T= (PRSS23)
ENST00000532234.5:c.*65-3871T= (PRSS23) ENSP00000436676.1:n.*65-3871T=
ENST00000533902.2:c.207-4731T= (PRSS23) ENSP00000437268.1:n.207-4731T=
NM_012193.3:c.*4657A= (FZD4) NP_036325.2:n.*4657A=
NR_120591.1:n.737-3871T= (PRSS23)
NR_120592.1:n.630-4731T= (PRSS23)
NR_120591.2:n.435-3871T= (PRSS23)
NR_120592.2:n.328-4731T= (PRSS23)
NM_012193.4:c.*4657A= (FZD4) MANE Select NP_036325.2:n.*4657A=
NR_120591.3:n.435-3871T= (PRSS23)