Canonical Allele Identifier: CA1988807678

Gene: FZD4 PRSS23

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.86951247_86951249delinsCGT , CM000673.2:g.86951247_86951249delinsCGT	GRCh38
NC_000011.9:g.86662289_86662291delinsCGT , CM000673.1:g.86662289_86662291delinsCGT	GRCh37
NC_000011.8:g.86339937_86339939delinsCGT	NCBI36
NG_011752.1:g.9143_9145delinsACG

Transcript Alleles

HGVS	Amino-acid change
ENST00000531380.2:c.1507_1509delinsACG (FZD4) MANE Select	ENSP00000434034.1:p.Thr503=
ENST00000528769.5:n.304_306delinsCGT (PRSS23)
ENST00000531380.1:c.1507_1509delinsACG (FZD4)	ENSP00000434034.1:p.Thr503=
ENST00000531521.1:n.418_420delinsCGT (PRSS23)
ENST00000532234.5:c.*240_*242delinsCGT (PRSS23)	ENSP00000436676.1:n.*240_*242delinsCGT
ENST00000533902.2:c.238_240delinsCGT (PRSS23)	ENSP00000437268.1:p.Arg80=
NM_012193.3:c.1507_1509delinsACG (FZD4)	NP_036325.2:p.Thr503=
NR_120591.1:n.912_914delinsCGT (PRSS23)
NR_120592.1:n.661_663delinsCGT (PRSS23)
NR_120591.2:n.610_612delinsCGT (PRSS23)
NR_120592.2:n.359_361delinsCGT (PRSS23)
NM_012193.4:c.1507_1509delinsACG (FZD4) MANE Select	NP_036325.2:p.Thr503=
NR_120591.3:n.610_612delinsCGT (PRSS23)