Canonical Allele Identifier: CA2615455785

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86946495A>G , CM000673.2:g.86946495A>G GRCh38
NC_000011.9:g.86657537A>G , CM000673.1:g.86657537A>G GRCh37
NC_000011.8:g.86335185A>G NCBI36
NG_011752.1:g.13897T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.*4647T>C (FZD4) MANE Select ENSP00000434034.1:n.*4647T>C
ENST00000528769.5:n.129-3861A>G (PRSS23)
ENST00000531380.1:c.*4647T>C (FZD4) ENSP00000434034.1:n.*4647T>C
ENST00000531521.1:n.243-3861A>G (PRSS23)
ENST00000532234.5:c.*65-3861A>G (PRSS23) ENSP00000436676.1:n.*65-3861A>G
ENST00000533902.2:c.207-4721A>G (PRSS23) ENSP00000437268.1:n.207-4721A>G
NM_012193.3:c.*4647T>C (FZD4) NP_036325.2:n.*4647T>C
NR_120591.1:n.737-3861A>G (PRSS23)
NR_120592.1:n.630-4721A>G (PRSS23)
NR_120591.2:n.435-3861A>G (PRSS23)
NR_120592.2:n.328-4721A>G (PRSS23)
NM_012193.4:c.*4647T>C (FZD4) MANE Select NP_036325.2:n.*4647T>C
NR_120591.3:n.435-3861A>G (PRSS23)