Canonical Allele Identifier: CA1988803996

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86947827_86947828delinsGT , CM000673.2:g.86947827_86947828delinsGT GRCh38
NC_000011.9:g.86658869_86658870delinsGT , CM000673.1:g.86658869_86658870delinsGT GRCh37
NC_000011.8:g.86336517_86336518delinsGT NCBI36
NG_011752.1:g.12564_12565delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.*3314_*3315delinsAC (FZD4) MANE Select ENSP00000434034.1:n.*3314_*3315delinsAC
ENST00000528769.5:n.129-2529_129-2528delinsGT (PRSS23)
ENST00000531380.1:c.*3314_*3315delinsAC (FZD4) ENSP00000434034.1:n.*3314_*3315delinsAC
ENST00000531521.1:n.243-2529_243-2528delinsGT (PRSS23)
ENST00000532234.5:c.*65-2529_*65-2528delinsGT (PRSS23) ENSP00000436676.1:n.*65-2529_*65-2528delinsGT
ENST00000533902.2:c.207-3389_207-3388delinsGT (PRSS23) ENSP00000437268.1:n.207-3389_207-3388delinsGT
NM_012193.3:c.*3314_*3315delinsAC (FZD4) NP_036325.2:n.*3314_*3315delinsAC
NR_120591.1:n.737-2529_737-2528delinsGT (PRSS23)
NR_120592.1:n.630-3389_630-3388delinsGT (PRSS23)
NR_120591.2:n.435-2529_435-2528delinsGT (PRSS23)
NR_120592.2:n.328-3389_328-3388delinsGT (PRSS23)
NM_012193.4:c.*3314_*3315delinsAC (FZD4) MANE Select NP_036325.2:n.*3314_*3315delinsAC
NR_120591.3:n.435-2529_435-2528delinsGT (PRSS23)