Canonical Allele Identifier: CA2615455800

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86946505C>A , CM000673.2:g.86946505C>A GRCh38
NC_000011.9:g.86657547C>A , CM000673.1:g.86657547C>A GRCh37
NC_000011.8:g.86335195C>A NCBI36
NG_011752.1:g.13887G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.*4637G>T (FZD4) MANE Select ENSP00000434034.1:n.*4637G>T
ENST00000528769.5:n.129-3851C>A (PRSS23)
ENST00000531380.1:c.*4637G>T (FZD4) ENSP00000434034.1:n.*4637G>T
ENST00000531521.1:n.243-3851C>A (PRSS23)
ENST00000532234.5:c.*65-3851C>A (PRSS23) ENSP00000436676.1:n.*65-3851C>A
ENST00000533902.2:c.207-4711C>A (PRSS23) ENSP00000437268.1:n.207-4711C>A
NM_012193.3:c.*4637G>T (FZD4) NP_036325.2:n.*4637G>T
NR_120591.1:n.737-3851C>A (PRSS23)
NR_120592.1:n.630-4711C>A (PRSS23)
NR_120591.2:n.435-3851C>A (PRSS23)
NR_120592.2:n.328-4711C>A (PRSS23)
NM_012193.4:c.*4637G>T (FZD4) MANE Select NP_036325.2:n.*4637G>T
NR_120591.3:n.435-3851C>A (PRSS23)