Canonical Allele Identifier: CA382011756

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951434G>T , CM000673.2:g.86951434G>T GRCh38
NC_000011.9:g.86662476G>T , CM000673.1:g.86662476G>T GRCh37
NC_000011.8:g.86340124G>T NCBI36
NG_011752.1:g.8958C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.1322C>A (FZD4) MANE Select ENSP00000434034.1:p.Ser441Ter
ENST00000531380.1:c.1322C>A (FZD4) ENSP00000434034.1:p.Ser441Ter
ENST00000531521.1:n.605G>T (PRSS23)
ENST00000532234.5:c.*427G>T (PRSS23) ENSP00000436676.1:n.*427G>T
ENST00000533902.2:c.*149G>T (PRSS23) ENSP00000437268.1:n.*149G>T
NM_012193.3:c.1322C>A (FZD4) NP_036325.2:p.Ser441Ter
NR_120591.1:n.1099G>T (PRSS23)
NR_120592.1:n.848G>T (PRSS23)
NR_120591.2:n.797G>T (PRSS23)
NR_120592.2:n.546G>T (PRSS23)
NM_012193.4:c.1322C>A (FZD4) MANE Select NP_036325.2:p.Ser441Ter
NR_120591.3:n.797G>T (PRSS23)