Canonical Allele Identifier: CA476144400

Linked Data

MyVariant Identifiers: chr11:g.86662520C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951478C>T , CM000673.2:g.86951478C>T GRCh38
NC_000011.9:g.86662520C>T , CM000673.1:g.86662520C>T GRCh37
NC_000011.8:g.86340168C>T NCBI36
NG_011752.1:g.8914G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.1278G>A (FZD4) MANE Select ENSP00000434034.1:p.Lys426=
ENST00000531380.1:c.1278G>A (FZD4) ENSP00000434034.1:p.Lys426=
ENST00000531521.1:n.649C>T (PRSS23)
ENST00000532234.5:c.*471C>T (PRSS23) ENSP00000436676.1:n.*471C>T
ENST00000533902.2:c.*193C>T (PRSS23) ENSP00000437268.1:n.*193C>T
NM_012193.3:c.1278G>A (FZD4) NP_036325.2:p.Lys426=
NR_120591.1:n.1143C>T (PRSS23)
NR_120592.1:n.892C>T (PRSS23)
NR_120591.2:n.841C>T (PRSS23)
NR_120592.2:n.590C>T (PRSS23)
NM_012193.4:c.1278G>A (FZD4) MANE Select NP_036325.2:p.Lys426=
NR_120591.3:n.841C>T (PRSS23)