Canonical Allele Identifier: CA1988807742

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951271_86951277delinsAATCCAC , CM000673.2:g.86951271_86951277delinsAATCCAC GRCh38
NC_000011.9:g.86662313_86662319delinsAATCCAC , CM000673.1:g.86662313_86662319delinsAATCCAC GRCh37
NC_000011.8:g.86339961_86339967delinsAATCCAC NCBI36
NG_011752.1:g.9115_9121delinsGTGGATT

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.1479_1485delinsGTGGATT (FZD4) MANE Select ENSP00000434034.1:p.Met493=
ENST00000528769.5:n.328_334delinsAATCCAC (PRSS23)
ENST00000531380.1:c.1479_1485delinsGTGGATT (FZD4) ENSP00000434034.1:p.Met493=
ENST00000531521.1:n.442_448delinsAATCCAC (PRSS23)
ENST00000532234.5:c.*264_*270delinsAATCCAC (PRSS23) ENSP00000436676.1:n.*264_*270delinsAATCCA...
ENST00000533902.2:c.262_268delinsAATCCAC (PRSS23) ENSP00000437268.1:p.Asn88=
NM_012193.3:c.1479_1485delinsGTGGATT (FZD4) NP_036325.2:p.Met493=
NR_120591.1:n.936_942delinsAATCCAC (PRSS23)
NR_120592.1:n.685_691delinsAATCCAC (PRSS23)
NR_120591.2:n.634_640delinsAATCCAC (PRSS23)
NR_120592.2:n.383_389delinsAATCCAC (PRSS23)
NM_012193.4:c.1479_1485delinsGTGGATT (FZD4) MANE Select NP_036325.2:p.Met493=
NR_120591.3:n.634_640delinsAATCCAC (PRSS23)