Canonical Allele Identifier: CA382011661

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951419A>G , CM000673.2:g.86951419A>G GRCh38
NC_000011.9:g.86662461A>G , CM000673.1:g.86662461A>G GRCh37
NC_000011.8:g.86340109A>G NCBI36
NG_011752.1:g.8973T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.1337T>C (FZD4) MANE Select ENSP00000434034.1:p.Val446Ala
ENST00000531380.1:c.1337T>C (FZD4) ENSP00000434034.1:p.Val446Ala
ENST00000531521.1:n.590A>G (PRSS23)
ENST00000532234.5:c.*412A>G (PRSS23) ENSP00000436676.1:n.*412A>G
ENST00000533902.2:c.*134A>G (PRSS23) ENSP00000437268.1:n.*134A>G
NM_012193.3:c.1337T>C (FZD4) NP_036325.2:p.Val446Ala
NR_120591.1:n.1084A>G (PRSS23)
NR_120592.1:n.833A>G (PRSS23)
NR_120591.2:n.782A>G (PRSS23)
NR_120592.2:n.531A>G (PRSS23)
NM_012193.4:c.1337T>C (FZD4) MANE Select NP_036325.2:p.Val446Ala
NR_120591.3:n.782A>G (PRSS23)