Canonical Allele Identifier: CA476144500

Linked Data

dbSNP Id: rs562056288

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951630A>G , CM000673.2:g.86951630A>G GRCh38
NC_000011.9:g.86662672A>G , CM000673.1:g.86662672A>G GRCh37
NC_000011.8:g.86340320A>G NCBI36
NG_011752.1:g.8762T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.1126T>C (FZD4) MANE Select ENSP00000434034.1:p.Leu376=
ENST00000531380.1:c.1126T>C (FZD4) ENSP00000434034.1:p.Leu376=
ENST00000531521.1:n.801A>G (PRSS23)
ENST00000532234.5:c.*623A>G (PRSS23) ENSP00000436676.1:n.*623A>G
ENST00000533902.2:c.*345A>G (PRSS23) ENSP00000437268.1:n.*345A>G
NM_012193.3:c.1126T>C (FZD4) NP_036325.2:p.Leu376=
NR_120591.1:n.1295A>G (PRSS23)
NR_120592.1:n.1044A>G (PRSS23)
NR_120591.2:n.993A>G (PRSS23)
NR_120592.2:n.742A>G (PRSS23)
NM_012193.4:c.1126T>C (FZD4) MANE Select NP_036325.2:p.Leu376=
NR_120591.3:n.993A>G (PRSS23)