Canonical Allele Identifier: CA1988808462

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951798_86951799delinsAC , CM000673.2:g.86951798_86951799delinsAC GRCh38
NC_000011.9:g.86662840_86662841delinsAC , CM000673.1:g.86662840_86662841delinsAC GRCh37
NC_000011.8:g.86340488_86340489delinsAC NCBI36
NG_011752.1:g.8593_8594delinsGT

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.957_958delinsGT (FZD4) MANE Select ENSP00000434034.1:p.Trp319=
ENST00000531380.1:c.957_958delinsGT (FZD4) ENSP00000434034.1:p.Trp319=
ENST00000532234.5:c.*791_*792delinsAC (PRSS23) ENSP00000436676.1:n.*791_*792delinsAC
ENST00000533902.2:c.*513_*514delinsAC (PRSS23) ENSP00000437268.1:n.*513_*514delinsAC
NM_012193.3:c.957_958delinsGT (FZD4) NP_036325.2:p.Trp319=
NR_120591.1:n.1463_1464delinsAC (PRSS23)
NR_120592.1:n.1212_1213delinsAC (PRSS23)
NR_120591.2:n.1161_1162delinsAC (PRSS23)
NR_120592.2:n.910_911delinsAC (PRSS23)
NM_012193.4:c.957_958delinsGT (FZD4) MANE Select NP_036325.2:p.Trp319=
NR_120591.3:n.1161_1162delinsAC (PRSS23)