Canonical Allele Identifier: CA476145066

Linked Data

MyVariant Identifiers: chr11:g.86663240G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952198G>T , CM000673.2:g.86952198G>T GRCh38
NC_000011.9:g.86663240G>T , CM000673.1:g.86663240G>T GRCh37
NC_000011.8:g.86340888G>T NCBI36
NG_011752.1:g.8194C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.558C>A (FZD4) MANE Select ENSP00000434034.1:p.Thr186=
ENST00000531380.1:c.558C>A (FZD4) ENSP00000434034.1:p.Thr186=
ENST00000532234.5:c.*1191G>T (PRSS23) ENSP00000436676.1:n.*1191G>T
ENST00000533902.2:c.*913G>T (PRSS23) ENSP00000437268.1:n.*913G>T
NM_012193.3:c.558C>A (FZD4) NP_036325.2:p.Thr186=
NR_120591.1:n.1863G>T (PRSS23)
NR_120592.1:n.1612G>T (PRSS23)
NR_120591.2:n.1561G>T (PRSS23)
NR_120592.2:n.1310G>T (PRSS23)
NM_012193.4:c.558C>A (FZD4) MANE Select NP_036325.2:p.Thr186=
NR_120591.3:n.1561G>T (PRSS23)