Canonical Allele Identifier: CA382011348

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951346A>C , CM000673.2:g.86951346A>C GRCh38
NC_000011.9:g.86662388A>C , CM000673.1:g.86662388A>C GRCh37
NC_000011.8:g.86340036A>C NCBI36
NG_011752.1:g.9046T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.1410T>G (FZD4) MANE Select ENSP00000434034.1:p.Asp470Glu
ENST00000528769.5:n.403A>C (PRSS23)
ENST00000531380.1:c.1410T>G (FZD4) ENSP00000434034.1:p.Asp470Glu
ENST00000531521.1:n.517A>C (PRSS23)
ENST00000532234.5:c.*339A>C (PRSS23) ENSP00000436676.1:n.*339A>C
ENST00000533902.2:c.*61A>C (PRSS23) ENSP00000437268.1:n.*61A>C
NM_012193.3:c.1410T>G (FZD4) NP_036325.2:p.Asp470Glu
NR_120591.1:n.1011A>C (PRSS23)
NR_120592.1:n.760A>C (PRSS23)
NR_120591.2:n.709A>C (PRSS23)
NR_120592.2:n.458A>C (PRSS23)
NM_012193.4:c.1410T>G (FZD4) MANE Select NP_036325.2:p.Asp470Glu
NR_120591.3:n.709A>C (PRSS23)