Canonical Allele Identifier: CA1988809306

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952392_86952394delinsGAC , CM000673.2:g.86952392_86952394delinsGAC GRCh38
NC_000011.9:g.86663434_86663436delinsGAC , CM000673.1:g.86663434_86663436delinsGAC GRCh37
NC_000011.8:g.86341082_86341084delinsGAC NCBI36
NG_011752.1:g.7998_8000delinsGTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.362_364delinsGTC (FZD4) MANE Select ENSP00000434034.1:p.Cys121=
ENST00000531380.1:c.362_364delinsGTC (FZD4) ENSP00000434034.1:p.Cys121=
ENST00000532234.5:c.*1385_*1387delinsGAC (PRSS23) ENSP00000436676.1:n.*1385_*1387delinsGAC
ENST00000533902.2:c.*1107_*1109delinsGAC (PRSS23) ENSP00000437268.1:n.*1107_*1109delinsGAC
NM_012193.3:c.362_364delinsGTC (FZD4) NP_036325.2:p.Cys121=
NR_120591.1:n.2057_2059delinsGAC (PRSS23)
NR_120592.1:n.1806_1808delinsGAC (PRSS23)
NR_120591.2:n.1755_1757delinsGAC (PRSS23)
NR_120592.2:n.1504_1506delinsGAC (PRSS23)
NM_012193.4:c.362_364delinsGTC (FZD4) MANE Select NP_036325.2:p.Cys121=
NR_120591.3:n.1755_1757delinsGAC (PRSS23)