Canonical Allele Identifier: CA476144285

Linked Data

MyVariant Identifiers: chr11:g.86662283C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951241C>T , CM000673.2:g.86951241C>T GRCh38
NC_000011.9:g.86662283C>T , CM000673.1:g.86662283C>T GRCh37
NC_000011.8:g.86339931C>T NCBI36
NG_011752.1:g.9151G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.1515G>A (FZD4) MANE Select ENSP00000434034.1:p.Gln505=
ENST00000528769.5:n.298C>T (PRSS23)
ENST00000531380.1:c.1515G>A (FZD4) ENSP00000434034.1:p.Gln505=
ENST00000531521.1:n.412C>T (PRSS23)
ENST00000532234.5:c.*234C>T (PRSS23) ENSP00000436676.1:n.*234C>T
ENST00000533902.2:c.232C>T (PRSS23) ENSP00000437268.1:p.Leu78=
NM_012193.3:c.1515G>A (FZD4) NP_036325.2:p.Gln505=
NR_120591.1:n.906C>T (PRSS23)
NR_120592.1:n.655C>T (PRSS23)
NR_120591.2:n.604C>T (PRSS23)
NR_120592.2:n.353C>T (PRSS23)
NM_012193.4:c.1515G>A (FZD4) MANE Select NP_036325.2:p.Gln505=
NR_120591.3:n.604C>T (PRSS23)