Canonical Allele Identifier: CA382016752

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952355T>C , CM000673.2:g.86952355T>C GRCh38
NC_000011.9:g.86663397T>C , CM000673.1:g.86663397T>C GRCh37
NC_000011.8:g.86341045T>C NCBI36
NG_011752.1:g.8037A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.401A>G (FZD4) MANE Select ENSP00000434034.1:p.Glu134Gly
ENST00000531380.1:c.401A>G (FZD4) ENSP00000434034.1:p.Glu134Gly
ENST00000532234.5:c.*1348T>C (PRSS23) ENSP00000436676.1:n.*1348T>C
ENST00000533902.2:c.*1070T>C (PRSS23) ENSP00000437268.1:n.*1070T>C
NM_012193.3:c.401A>G (FZD4) NP_036325.2:p.Glu134Gly
NR_120591.1:n.2020T>C (PRSS23)
NR_120592.1:n.1769T>C (PRSS23)
NR_120591.2:n.1718T>C (PRSS23)
NR_120592.2:n.1467T>C (PRSS23)
NM_012193.4:c.401A>G (FZD4) MANE Select NP_036325.2:p.Glu134Gly
NR_120591.3:n.1718T>C (PRSS23)