Canonical Allele Identifier: CA2695215107

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951546_86951547del , CM000673.2:g.86951546_86951547del GRCh38
NC_000011.9:g.86662588_86662589del , CM000673.1:g.86662588_86662589del GRCh37
NC_000011.8:g.86340236_86340237del NCBI36
NG_011752.1:g.8846_8847del

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.1210_1211del (FZD4) MANE Select ENSP00000434034.1:p.Leu404ValfsTer?
ENST00000531380.1:c.1210_1211del (FZD4) ENSP00000434034.1:p.Leu404ValfsTer?
ENST00000531521.1:n.717_718del (PRSS23)
ENST00000532234.5:c.*539_*540del (PRSS23) ENSP00000436676.1:n.*539_*540del
ENST00000533902.2:c.*261_*262del (PRSS23) ENSP00000437268.1:n.*261_*262del
NM_012193.3:c.1210_1211del (FZD4) NP_036325.2:p.Leu404ValfsTer?
NR_120591.1:n.1211_1212del (PRSS23)
NR_120592.1:n.960_961del (PRSS23)
NR_120591.2:n.909_910del (PRSS23)
NR_120592.2:n.658_659del (PRSS23)
NM_012193.4:c.1210_1211del (FZD4) MANE Select NP_036325.2:p.Leu404ValfsTer?
NR_120591.3:n.909_910del (PRSS23)