Canonical Allele Identifier: CA2615455648

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86946417_86946421del , CM000673.2:g.86946417_86946421del GRCh38
NC_000011.9:g.86657459_86657463del , CM000673.1:g.86657459_86657463del GRCh37
NC_000011.8:g.86335107_86335111del NCBI36
NG_011752.1:g.13971_13975del

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.*4721_*4725del (FZD4) MANE Select ENSP00000434034.1:n.*4721_*4725del
ENST00000528769.5:n.129-3939_129-3935del (PRSS23)
ENST00000531380.1:c.*4721_*4725del (FZD4) ENSP00000434034.1:n.*4721_*4725del
ENST00000531521.1:n.243-3939_243-3935del (PRSS23)
ENST00000532234.5:c.*65-3939_*65-3935del (PRSS23) ENSP00000436676.1:n.*65-3939_*65-3935del
ENST00000533902.2:c.207-4799_207-4795del (PRSS23) ENSP00000437268.1:n.207-4799_207-4795del
NM_012193.3:c.*4721_*4725del (FZD4) NP_036325.2:n.*4721_*4725del
NR_120591.1:n.737-3939_737-3935del (PRSS23)
NR_120592.1:n.630-4799_630-4795del (PRSS23)
NR_120591.2:n.435-3939_435-3935del (PRSS23)
NR_120592.2:n.328-4799_328-4795del (PRSS23)
NM_012193.4:c.*4721_*4725del (FZD4) MANE Select NP_036325.2:n.*4721_*4725del
NR_120591.3:n.435-3939_435-3935del (PRSS23)