Canonical Allele Identifier: CA382011483

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951384C>G , CM000673.2:g.86951384C>G GRCh38
NC_000011.9:g.86662426C>G , CM000673.1:g.86662426C>G GRCh37
NC_000011.8:g.86340074C>G NCBI36
NG_011752.1:g.9008G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.1372G>C (FZD4) MANE Select ENSP00000434034.1:p.Glu458Gln
ENST00000528769.5:n.441C>G (PRSS23)
ENST00000531380.1:c.1372G>C (FZD4) ENSP00000434034.1:p.Glu458Gln
ENST00000531521.1:n.555C>G (PRSS23)
ENST00000532234.5:c.*377C>G (PRSS23) ENSP00000436676.1:n.*377C>G
ENST00000533902.2:c.*99C>G (PRSS23) ENSP00000437268.1:n.*99C>G
NM_012193.3:c.1372G>C (FZD4) NP_036325.2:p.Glu458Gln
NR_120591.1:n.1049C>G (PRSS23)
NR_120592.1:n.798C>G (PRSS23)
NR_120591.2:n.747C>G (PRSS23)
NR_120592.2:n.496C>G (PRSS23)
NM_012193.4:c.1372G>C (FZD4) MANE Select NP_036325.2:p.Glu458Gln
NR_120591.3:n.747C>G (PRSS23)