Canonical Allele Identifier: CA1988804007

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86947849_86947867delinsCTCTGGAGGCCAAGGGATT , CM000673.2:g.86947849_86947867delinsCTCTGGAGGCCAAGGGATT GRCh38
NC_000011.9:g.86658891_86658909delinsCTCTGGAGGCCAAGGGATT , CM000673.1:g.86658891_86658909delinsCTCTGGAGGCCAAGGGATT GRCh37
NC_000011.8:g.86336539_86336557delinsCTCTGGAGGCCAAGGGATT NCBI36
NG_011752.1:g.12525_12543delinsAATCCCTTGGCCTCCAGAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.*3275_*3293delinsAATCCCTTGGCCTCCAGAG (FZD4) MANE Select ENSP00000434034.1:n.*3275_*3293delinsAATCCCTTGGCCTCCAGAG
ENST00000528769.5:n.129-2507_129-2489delinsCTCTGGAGGCCAAGGGATT (PRSS23)
ENST00000531380.1:c.*3275_*3293delinsAATCCCTTGGCCTCCAGAG (FZD4) ENSP00000434034.1:n.*3275_*3293delinsAATCCCTTGGCCTCCAGAG
ENST00000531521.1:n.243-2507_243-2489delinsCTCTGGAGGCCAAGGGATT (PRSS23)
ENST00000532234.5:c.*65-2507_*65-2489delinsCTCTGGAGGCCAAGGGATT (PRSS23) ENSP00000436676.1:n.*65-2507_*65-2489delinsCTCTGGAGGCCAAGGGAT...
ENST00000533902.2:c.207-3367_207-3349delinsCTCTGGAGGCCAAGGGATT (PRSS23) ENSP00000437268.1:n.207-3367_207-3349delinsCTCTGGAGGCCAAGGGAT...
NM_012193.3:c.*3275_*3293delinsAATCCCTTGGCCTCCAGAG (FZD4) NP_036325.2:n.*3275_*3293delinsAATCCCTTGGCCTCCAGAG
NR_120591.1:n.737-2507_737-2489delinsCTCTGGAGGCCAAGGGATT (PRSS23)
NR_120592.1:n.630-3367_630-3349delinsCTCTGGAGGCCAAGGGATT (PRSS23)
NR_120591.2:n.435-2507_435-2489delinsCTCTGGAGGCCAAGGGATT (PRSS23)
NR_120592.2:n.328-3367_328-3349delinsCTCTGGAGGCCAAGGGATT (PRSS23)
NM_012193.4:c.*3275_*3293delinsAATCCCTTGGCCTCCAGAG (FZD4) MANE Select NP_036325.2:n.*3275_*3293delinsAATCCCTTGGCCTCCAGAG
NR_120591.3:n.435-2507_435-2489delinsCTCTGGAGGCCAAGGGATT (PRSS23)