Canonical Allele Identifier: CA476144340

Linked Data

MyVariant Identifiers: chr11:g.86662421G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951379G>A , CM000673.2:g.86951379G>A GRCh38
NC_000011.9:g.86662421G>A , CM000673.1:g.86662421G>A GRCh37
NC_000011.8:g.86340069G>A NCBI36
NG_011752.1:g.9013C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.1377C>T (FZD4) MANE Select ENSP00000434034.1:p.Ile459=
ENST00000528769.5:n.436G>A (PRSS23)
ENST00000531380.1:c.1377C>T (FZD4) ENSP00000434034.1:p.Ile459=
ENST00000531521.1:n.550G>A (PRSS23)
ENST00000532234.5:c.*372G>A (PRSS23) ENSP00000436676.1:n.*372G>A
ENST00000533902.2:c.*94G>A (PRSS23) ENSP00000437268.1:n.*94G>A
NM_012193.3:c.1377C>T (FZD4) NP_036325.2:p.Ile459=
NR_120591.1:n.1044G>A (PRSS23)
NR_120592.1:n.793G>A (PRSS23)
NR_120591.2:n.742G>A (PRSS23)
NR_120592.2:n.491G>A (PRSS23)
NM_012193.4:c.1377C>T (FZD4) MANE Select NP_036325.2:p.Ile459=
NR_120591.3:n.742G>A (PRSS23)