Canonical Allele Identifier: CA1988809418
Community Standard Title: NM_012193.4(FZD4):c.314T= (p.Met105=)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952442A= , CM000673.2:g.86952442A= GRCh38
NC_000011.9:g.86663484A= , CM000673.1:g.86663484A= GRCh37
NC_000011.8:g.86341132A= NCBI36
NG_011752.1:g.7950T=

Transcript Alleles

HGVS Amino-acid Change
NM_012193.4:c.314T= (FZD4) MANE Select NP_036325.2:p.Met105=
ENST00000531380.2:c.314T= (FZD4) MANE Select ENSP00000434034.1:p.Met105=
NM_012193.3:c.314T= (FZD4) NP_036325.2:p.Met105=
NR_120591.1:n.2107A= (PRSS23)
NR_120591.2:n.1805A= (PRSS23)
NR_120591.3:n.1805A= (PRSS23)
NR_120592.1:n.1856A= (PRSS23)
NR_120592.2:n.1554A= (PRSS23)
ENST00000531380.1:c.314T= (FZD4) ENSP00000434034.1:p.Met105=
ENST00000532234.5:c.*1435A= (PRSS23) ENSP00000436676.1:n.*1435A=
ENST00000533902.2:c.*1157A= (PRSS23) ENSP00000437268.1:n.*1157A=