Canonical Allele Identifier: CA1988807997
Community Standard Title: NM_012193.4(FZD4):c.1333A= (p.Thr445=)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951423T= , CM000673.2:g.86951423T= GRCh38
NC_000011.9:g.86662465T= , CM000673.1:g.86662465T= GRCh37
NC_000011.8:g.86340113T= NCBI36
NG_011752.1:g.8969A=

Transcript Alleles

HGVS Amino-acid Change
NM_012193.4:c.1333A= (FZD4) MANE Select NP_036325.2:p.Thr445=
ENST00000531380.2:c.1333A= (FZD4) MANE Select ENSP00000434034.1:p.Thr445=
NM_012193.3:c.1333A= (FZD4) NP_036325.2:p.Thr445=
NR_120591.1:n.1088T= (PRSS23)
NR_120591.2:n.786T= (PRSS23)
NR_120591.3:n.786T= (PRSS23)
NR_120592.1:n.837T= (PRSS23)
NR_120592.2:n.535T= (PRSS23)
ENST00000531380.1:c.1333A= (FZD4) ENSP00000434034.1:p.Thr445=
ENST00000531521.1:n.594T= (PRSS23)
ENST00000532234.5:c.*416T= (PRSS23) ENSP00000436676.1:n.*416T=
ENST00000533902.2:c.*138T= (PRSS23) ENSP00000437268.1:n.*138T=