Canonical Allele Identifier: CA1988809459

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952467_86952468delinsAG , CM000673.2:g.86952467_86952468delinsAG GRCh38
NC_000011.9:g.86663509_86663510delinsAG , CM000673.1:g.86663509_86663510delinsAG GRCh37
NC_000011.8:g.86341157_86341158delinsAG NCBI36
NG_011752.1:g.7924_7925delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.288_289delinsCT (FZD4) MANE Select ENSP00000434034.1:p.Phe96=
ENST00000531380.1:c.288_289delinsCT (FZD4) ENSP00000434034.1:p.Phe96=
ENST00000532234.5:c.*1460_*1461delinsAG (PRSS23) ENSP00000436676.1:n.*1460_*1461delinsAG
ENST00000533902.2:c.*1182_*1183delinsAG (PRSS23) ENSP00000437268.1:n.*1182_*1183delinsAG
NM_012193.3:c.288_289delinsCT (FZD4) NP_036325.2:p.Phe96=
NR_120591.1:n.2132_2133delinsAG (PRSS23)
NR_120592.1:n.1881_1882delinsAG (PRSS23)
NR_120591.2:n.1830_1831delinsAG (PRSS23)
NR_120592.2:n.1579_1580delinsAG (PRSS23)
NM_012193.4:c.288_289delinsCT (FZD4) MANE Select NP_036325.2:p.Phe96=
NR_120591.3:n.1830_1831delinsAG (PRSS23)