Canonical Allele Identifier: CA1988809465

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952474G= , CM000673.2:g.86952474G= GRCh38
NC_000011.9:g.86663516G= , CM000673.1:g.86663516G= GRCh37
NC_000011.8:g.86341164G= NCBI36
NG_011752.1:g.7918C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.286-4C= (FZD4) MANE Select ENSP00000434034.1:n.286-4C=
ENST00000531380.1:c.286-4C= (FZD4) ENSP00000434034.1:n.286-4C=
ENST00000532234.5:c.*1467G= (PRSS23) ENSP00000436676.1:n.*1467G=
ENST00000533902.2:c.*1189G= (PRSS23) ENSP00000437268.1:n.*1189G=
NM_012193.3:c.286-4C= (FZD4) NP_036325.2:n.286-4C=
NR_120591.1:n.2139G= (PRSS23)
NR_120592.1:n.1888G= (PRSS23)
NR_120591.2:n.1837G= (PRSS23)
NR_120592.2:n.1586G= (PRSS23)
NM_012193.4:c.286-4C= (FZD4) MANE Select NP_036325.2:n.286-4C=
NR_120591.3:n.1837G= (PRSS23)