Canonical Allele Identifier: CA2615456513

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952520G>T , CM000673.2:g.86952520G>T GRCh38
NC_000011.9:g.86663562G>T , CM000673.1:g.86663562G>T GRCh37
NC_000011.8:g.86341210G>T NCBI36
NG_011752.1:g.7872C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.286-50C>A (FZD4) MANE Select ENSP00000434034.1:n.286-50C>A
ENST00000531380.1:c.286-50C>A (FZD4) ENSP00000434034.1:n.286-50C>A
ENST00000532234.5:c.*1513G>T (PRSS23) ENSP00000436676.1:n.*1513G>T
ENST00000533902.2:c.*1235G>T (PRSS23) ENSP00000437268.1:n.*1235G>T
NM_012193.3:c.286-50C>A (FZD4) NP_036325.2:n.286-50C>A
NR_120591.1:n.2185G>T (PRSS23)
NR_120592.1:n.1934G>T (PRSS23)
NR_120591.2:n.1883G>T (PRSS23)
NR_120592.2:n.1632G>T (PRSS23)
NM_012193.4:c.286-50C>A (FZD4) MANE Select NP_036325.2:n.286-50C>A
NR_120591.3:n.1883G>T (PRSS23)