Canonical Allele Identifier: CA382013041

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951639G>C , CM000673.2:g.86951639G>C GRCh38
NC_000011.9:g.86662681G>C , CM000673.1:g.86662681G>C GRCh37
NC_000011.8:g.86340329G>C NCBI36
NG_011752.1:g.8753C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.1117C>G (FZD4) MANE Select ENSP00000434034.1:p.Leu373Val
ENST00000531380.1:c.1117C>G (FZD4) ENSP00000434034.1:p.Leu373Val
ENST00000531521.1:n.810G>C (PRSS23)
ENST00000532234.5:c.*632G>C (PRSS23) ENSP00000436676.1:n.*632G>C
ENST00000533902.2:c.*354G>C (PRSS23) ENSP00000437268.1:n.*354G>C
NM_012193.3:c.1117C>G (FZD4) NP_036325.2:p.Leu373Val
NR_120591.1:n.1304G>C (PRSS23)
NR_120592.1:n.1053G>C (PRSS23)
NR_120591.2:n.1002G>C (PRSS23)
NR_120592.2:n.751G>C (PRSS23)
NM_012193.4:c.1117C>G (FZD4) MANE Select NP_036325.2:p.Leu373Val
NR_120591.3:n.1002G>C (PRSS23)