Canonical Allele Identifier: CA382013093

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951645C>A , CM000673.2:g.86951645C>A GRCh38
NC_000011.9:g.86662687C>A , CM000673.1:g.86662687C>A GRCh37
NC_000011.8:g.86340335C>A NCBI36
NG_011752.1:g.8747G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.1111G>T (FZD4) MANE Select ENSP00000434034.1:p.Asp371Tyr
ENST00000531380.1:c.1111G>T (FZD4) ENSP00000434034.1:p.Asp371Tyr
ENST00000531521.1:n.816C>A (PRSS23)
ENST00000532234.5:c.*638C>A (PRSS23) ENSP00000436676.1:n.*638C>A
ENST00000533902.2:c.*360C>A (PRSS23) ENSP00000437268.1:n.*360C>A
NM_012193.3:c.1111G>T (FZD4) NP_036325.2:p.Asp371Tyr
NR_120591.1:n.1310C>A (PRSS23)
NR_120592.1:n.1059C>A (PRSS23)
NR_120591.2:n.1008C>A (PRSS23)
NR_120592.2:n.757C>A (PRSS23)
NM_012193.4:c.1111G>T (FZD4) MANE Select NP_036325.2:p.Asp371Tyr
NR_120591.3:n.1008C>A (PRSS23)