Canonical Allele Identifier: CA1988808716
Community Standard Title: NM_012193.4(FZD4):c.766A= (p.Ile256=)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951990T= , CM000673.2:g.86951990T= GRCh38
NC_000011.9:g.86663032T= , CM000673.1:g.86663032T= GRCh37
NC_000011.8:g.86340680T= NCBI36
NG_011752.1:g.8402A=

Transcript Alleles

HGVS Amino-acid Change
NM_012193.4:c.766A= (FZD4) MANE Select NP_036325.2:p.Ile256=
ENST00000531380.2:c.766A= (FZD4) MANE Select ENSP00000434034.1:p.Ile256=
NM_012193.3:c.766A= (FZD4) NP_036325.2:p.Ile256=
NR_120591.1:n.1655T= (PRSS23)
NR_120591.2:n.1353T= (PRSS23)
NR_120591.3:n.1353T= (PRSS23)
NR_120592.1:n.1404T= (PRSS23)
NR_120592.2:n.1102T= (PRSS23)
ENST00000531380.1:c.766A= (FZD4) ENSP00000434034.1:p.Ile256=
ENST00000532234.5:c.*983T= (PRSS23) ENSP00000436676.1:n.*983T=
ENST00000533902.2:c.*705T= (PRSS23) ENSP00000437268.1:n.*705T=