Canonical Allele Identifier: CA2793028385

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952538_86952539insGTG , CM000673.2:g.86952538_86952539insGTG GRCh38
NC_000011.9:g.86663580_86663581insGTG , CM000673.1:g.86663580_86663581insGTG GRCh37
NC_000011.8:g.86341228_86341229insGTG NCBI36
NG_011752.1:g.7853_7854insCAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.286-69_286-68insCAC (FZD4) MANE Select ENSP00000434034.1:n.286-69_286-68insCAC
ENST00000531380.1:c.286-69_286-68insCAC (FZD4) ENSP00000434034.1:n.286-69_286-68insCAC
ENST00000532234.5:c.*1531_*1532insGTG (PRSS23) ENSP00000436676.1:n.*1531_*1532insGTG
ENST00000533902.2:c.*1253_*1254insGTG (PRSS23) ENSP00000437268.1:n.*1253_*1254insGTG
NM_012193.3:c.286-69_286-68insCAC (FZD4) NP_036325.2:n.286-69_286-68insCAC
NR_120591.1:n.2203_2204insGTG (PRSS23)
NR_120592.1:n.1952_1953insGTG (PRSS23)
NR_120591.2:n.1901_1902insGTG (PRSS23)
NR_120592.2:n.1650_1651insGTG (PRSS23)
NM_012193.4:c.286-69_286-68insCAC (FZD4) MANE Select NP_036325.2:n.286-69_286-68insCAC
NR_120591.3:n.1901_1902insGTG (PRSS23)