Canonical Allele Identifier: CA1988804228

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86948056_86948063delinsAGTCTTCC , CM000673.2:g.86948056_86948063delinsAGTCTTCC GRCh38
NC_000011.9:g.86659098_86659105delinsAGTCTTCC , CM000673.1:g.86659098_86659105delinsAGTCTTCC GRCh37
NC_000011.8:g.86336746_86336753delinsAGTCTTCC NCBI36
NG_011752.1:g.12329_12336delinsGGAAGACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.*3079_*3086delinsGGAAGACT (FZD4) MANE Select ENSP00000434034.1:n.*3079_*3086delinsGGAAGACT
ENST00000528769.5:n.129-2300_129-2293delinsAGTCTTCC (PRSS23)
ENST00000531380.1:c.*3079_*3086delinsGGAAGACT (FZD4) ENSP00000434034.1:n.*3079_*3086delinsGGAAGACT
ENST00000531521.1:n.243-2300_243-2293delinsAGTCTTCC (PRSS23)
ENST00000532234.5:c.*65-2300_*65-2293delinsAGTCTTCC (PRSS23) ENSP00000436676.1:n.*65-2300_*65-2293delinsAGTCTTCC
ENST00000533902.2:c.207-3160_207-3153delinsAGTCTTCC (PRSS23) ENSP00000437268.1:n.207-3160_207-3153delinsAGTCTTCC
NM_012193.3:c.*3079_*3086delinsGGAAGACT (FZD4) NP_036325.2:n.*3079_*3086delinsGGAAGACT
NR_120591.1:n.737-2300_737-2293delinsAGTCTTCC (PRSS23)
NR_120592.1:n.630-3160_630-3153delinsAGTCTTCC (PRSS23)
NR_120591.2:n.435-2300_435-2293delinsAGTCTTCC (PRSS23)
NR_120592.2:n.328-3160_328-3153delinsAGTCTTCC (PRSS23)
NM_012193.4:c.*3079_*3086delinsGGAAGACT (FZD4) MANE Select NP_036325.2:n.*3079_*3086delinsGGAAGACT
NR_120591.3:n.435-2300_435-2293delinsAGTCTTCC (PRSS23)