Canonical Allele Identifier: CA382011280

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951326T>G , CM000673.2:g.86951326T>G GRCh38
NC_000011.9:g.86662368T>G , CM000673.1:g.86662368T>G GRCh37
NC_000011.8:g.86340016T>G NCBI36
NG_011752.1:g.9066A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.1430A>C (FZD4) MANE Select ENSP00000434034.1:p.Glu477Ala
ENST00000528769.5:n.383T>G (PRSS23)
ENST00000531380.1:c.1430A>C (FZD4) ENSP00000434034.1:p.Glu477Ala
ENST00000531521.1:n.497T>G (PRSS23)
ENST00000532234.5:c.*319T>G (PRSS23) ENSP00000436676.1:n.*319T>G
ENST00000533902.2:c.*41T>G (PRSS23) ENSP00000437268.1:n.*41T>G
NM_012193.3:c.1430A>C (FZD4) NP_036325.2:p.Glu477Ala
NR_120591.1:n.991T>G (PRSS23)
NR_120592.1:n.740T>G (PRSS23)
NR_120591.2:n.689T>G (PRSS23)
NR_120592.2:n.438T>G (PRSS23)
NM_012193.4:c.1430A>C (FZD4) MANE Select NP_036325.2:p.Glu477Ala
NR_120591.3:n.689T>G (PRSS23)