Canonical Allele Identifier: CA476144350

Linked Data

MyVariant Identifiers: chr11:g.86662442A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951400A>T , CM000673.2:g.86951400A>T GRCh38
NC_000011.9:g.86662442A>T , CM000673.1:g.86662442A>T GRCh37
NC_000011.8:g.86340090A>T NCBI36
NG_011752.1:g.8992T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.1356T>A (FZD4) MANE Select ENSP00000434034.1:p.Ile452=
ENST00000528769.5:n.457A>T (PRSS23)
ENST00000531380.1:c.1356T>A (FZD4) ENSP00000434034.1:p.Ile452=
ENST00000531521.1:n.571A>T (PRSS23)
ENST00000532234.5:c.*393A>T (PRSS23) ENSP00000436676.1:n.*393A>T
ENST00000533902.2:c.*115A>T (PRSS23) ENSP00000437268.1:n.*115A>T
NM_012193.3:c.1356T>A (FZD4) NP_036325.2:p.Ile452=
NR_120591.1:n.1065A>T (PRSS23)
NR_120592.1:n.814A>T (PRSS23)
NR_120591.2:n.763A>T (PRSS23)
NR_120592.2:n.512A>T (PRSS23)
NM_012193.4:c.1356T>A (FZD4) MANE Select NP_036325.2:p.Ile452=
NR_120591.3:n.763A>T (PRSS23)