Canonical Allele Identifier: CA1988807703

Gene: FZD4 PRSS23

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.86951253_86951255delinsAAG , CM000673.2:g.86951253_86951255delinsAAG	GRCh38
NC_000011.9:g.86662295_86662297delinsAAG , CM000673.1:g.86662295_86662297delinsAAG	GRCh37
NC_000011.8:g.86339943_86339945delinsAAG	NCBI36
NG_011752.1:g.9137_9139delinsCTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000531380.2:c.1501_1503delinsCTT (FZD4) MANE Select	ENSP00000434034.1:p.Leu501=
ENST00000528769.5:n.310_312delinsAAG (PRSS23)
ENST00000531380.1:c.1501_1503delinsCTT (FZD4)	ENSP00000434034.1:p.Leu501=
ENST00000531521.1:n.424_426delinsAAG (PRSS23)
ENST00000532234.5:c.*246_*248delinsAAG (PRSS23)	ENSP00000436676.1:n.*246_*248delinsAAG
ENST00000533902.2:c.244_246delinsAAG (PRSS23)	ENSP00000437268.1:p.Lys82=
NM_012193.3:c.1501_1503delinsCTT (FZD4)	NP_036325.2:p.Leu501=
NR_120591.1:n.918_920delinsAAG (PRSS23)
NR_120592.1:n.667_669delinsAAG (PRSS23)
NR_120591.2:n.616_618delinsAAG (PRSS23)
NR_120592.2:n.365_367delinsAAG (PRSS23)
NM_012193.4:c.1501_1503delinsCTT (FZD4) MANE Select	NP_036325.2:p.Leu501=
NR_120591.3:n.616_618delinsAAG (PRSS23)