Canonical Allele Identifier: CA225381530

Linked Data

dbSNP Id: rs911736787

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952336T>C , CM000673.2:g.86952336T>C GRCh38
NC_000011.9:g.86663378T>C , CM000673.1:g.86663378T>C GRCh37
NC_000011.8:g.86341026T>C NCBI36
NG_011752.1:g.8056A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.420A>G (FZD4) MANE Select ENSP00000434034.1:p.Pro140=
ENST00000531380.1:c.420A>G (FZD4) ENSP00000434034.1:p.Pro140=
ENST00000532234.5:c.*1329T>C (PRSS23) ENSP00000436676.1:n.*1329T>C
ENST00000533902.2:c.*1051T>C (PRSS23) ENSP00000437268.1:n.*1051T>C
NM_012193.3:c.420A>G (FZD4) NP_036325.2:p.Pro140=
NR_120591.1:n.2001T>C (PRSS23)
NR_120592.1:n.1750T>C (PRSS23)
NR_120591.2:n.1699T>C (PRSS23)
NR_120592.2:n.1448T>C (PRSS23)
NM_012193.4:c.420A>G (FZD4) MANE Select NP_036325.2:p.Pro140=
NR_120591.3:n.1699T>C (PRSS23)