Canonical Allele Identifier: CA1988807053

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86950767T= , CM000673.2:g.86950767T= GRCh38
NC_000011.9:g.86661809T= , CM000673.1:g.86661809T= GRCh37
NC_000011.8:g.86339457T= NCBI36
NG_011752.1:g.9625A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.*375A= (FZD4) MANE Select ENSP00000434034.1:n.*375A=
ENST00000528769.5:n.272+268T= (PRSS23)
ENST00000531380.1:c.*375A= (FZD4) ENSP00000434034.1:n.*375A=
ENST00000531521.1:n.386+268T= (PRSS23)
ENST00000532234.5:c.*208+268T= (PRSS23) ENSP00000436676.1:n.*208+268T=
ENST00000533902.2:c.207-449T= (PRSS23) ENSP00000437268.1:n.207-449T=
NM_012193.3:c.*375A= (FZD4) NP_036325.2:n.*375A=
NR_120591.1:n.880+268T= (PRSS23)
NR_120592.1:n.630-449T= (PRSS23)
NR_120591.2:n.578+268T= (PRSS23)
NR_120592.2:n.328-449T= (PRSS23)
NM_012193.4:c.*375A= (FZD4) MANE Select NP_036325.2:n.*375A=
NR_120591.3:n.578+268T= (PRSS23)