Canonical Allele Identifier: CA1988809092

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952229T= , CM000673.2:g.86952229T= GRCh38
NC_000011.9:g.86663271T= , CM000673.1:g.86663271T= GRCh37
NC_000011.8:g.86340919T= NCBI36
NG_011752.1:g.8163A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.527A= (FZD4) MANE Select ENSP00000434034.1:p.Gln176=
ENST00000531380.1:c.527A= (FZD4) ENSP00000434034.1:p.Gln176=
ENST00000532234.5:c.*1222T= (PRSS23) ENSP00000436676.1:n.*1222T=
ENST00000533902.2:c.*944T= (PRSS23) ENSP00000437268.1:n.*944T=
NM_012193.3:c.527A= (FZD4) NP_036325.2:p.Gln176=
NR_120591.1:n.1894T= (PRSS23)
NR_120592.1:n.1643T= (PRSS23)
NR_120591.2:n.1592T= (PRSS23)
NR_120592.2:n.1341T= (PRSS23)
NM_012193.4:c.527A= (FZD4) MANE Select NP_036325.2:p.Gln176=
NR_120591.3:n.1592T= (PRSS23)