Canonical Allele Identifier: CA2793028416

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952554_86952555insA , CM000673.2:g.86952554_86952555insA GRCh38
NC_000011.9:g.86663596_86663597insA , CM000673.1:g.86663596_86663597insA GRCh37
NC_000011.8:g.86341244_86341245insA NCBI36
NG_011752.1:g.7837_7838insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.286-85_286-84insT (FZD4) MANE Select ENSP00000434034.1:n.286-85_286-84insT
ENST00000531380.1:c.286-85_286-84insT (FZD4) ENSP00000434034.1:n.286-85_286-84insT
ENST00000532234.5:c.*1547_*1548insA (PRSS23) ENSP00000436676.1:n.*1547_*1548insA
ENST00000533902.2:c.*1269_*1270insA (PRSS23) ENSP00000437268.1:n.*1269_*1270insA
NM_012193.3:c.286-85_286-84insT (FZD4) NP_036325.2:n.286-85_286-84insT
NR_120591.1:n.2219_2220insA (PRSS23)
NR_120592.1:n.1968_1969insA (PRSS23)
NR_120591.2:n.1917_1918insA (PRSS23)
NR_120592.2:n.1666_1667insA (PRSS23)
NM_012193.4:c.286-85_286-84insT (FZD4) MANE Select NP_036325.2:n.286-85_286-84insT
NR_120591.3:n.1917_1918insA (PRSS23)