Canonical Allele Identifier: CA476144315

Linked Data

MyVariant Identifiers: chr11:g.86662373A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951331A>T , CM000673.2:g.86951331A>T GRCh38
NC_000011.9:g.86662373A>T , CM000673.1:g.86662373A>T GRCh37
NC_000011.8:g.86340021A>T NCBI36
NG_011752.1:g.9061T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.1425T>A (FZD4) MANE Select ENSP00000434034.1:p.Ala475=
ENST00000528769.5:n.388A>T (PRSS23)
ENST00000531380.1:c.1425T>A (FZD4) ENSP00000434034.1:p.Ala475=
ENST00000531521.1:n.502A>T (PRSS23)
ENST00000532234.5:c.*324A>T (PRSS23) ENSP00000436676.1:n.*324A>T
ENST00000533902.2:c.*46A>T (PRSS23) ENSP00000437268.1:n.*46A>T
NM_012193.3:c.1425T>A (FZD4) NP_036325.2:p.Ala475=
NR_120591.1:n.996A>T (PRSS23)
NR_120592.1:n.745A>T (PRSS23)
NR_120591.2:n.694A>T (PRSS23)
NR_120592.2:n.443A>T (PRSS23)
NM_012193.4:c.1425T>A (FZD4) MANE Select NP_036325.2:p.Ala475=
NR_120591.3:n.694A>T (PRSS23)