Canonical Allele Identifier: CA476144342

Linked Data

MyVariant Identifiers: chr11:g.86662424T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951382T>C , CM000673.2:g.86951382T>C GRCh38
NC_000011.9:g.86662424T>C , CM000673.1:g.86662424T>C GRCh37
NC_000011.8:g.86340072T>C NCBI36
NG_011752.1:g.9010A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.1374A>G (FZD4) MANE Select ENSP00000434034.1:p.Glu458=
ENST00000528769.5:n.439T>C (PRSS23)
ENST00000531380.1:c.1374A>G (FZD4) ENSP00000434034.1:p.Glu458=
ENST00000531521.1:n.553T>C (PRSS23)
ENST00000532234.5:c.*375T>C (PRSS23) ENSP00000436676.1:n.*375T>C
ENST00000533902.2:c.*97T>C (PRSS23) ENSP00000437268.1:n.*97T>C
NM_012193.3:c.1374A>G (FZD4) NP_036325.2:p.Glu458=
NR_120591.1:n.1047T>C (PRSS23)
NR_120592.1:n.796T>C (PRSS23)
NR_120591.2:n.745T>C (PRSS23)
NR_120592.2:n.494T>C (PRSS23)
NM_012193.4:c.1374A>G (FZD4) MANE Select NP_036325.2:p.Glu458=
NR_120591.3:n.745T>C (PRSS23)