Canonical Allele Identifier: CA382012632

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951576G>T , CM000673.2:g.86951576G>T GRCh38
NC_000011.9:g.86662618G>T , CM000673.1:g.86662618G>T GRCh37
NC_000011.8:g.86340266G>T NCBI36
NG_011752.1:g.8816C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.1180C>A (FZD4) MANE Select ENSP00000434034.1:p.Pro394Thr
ENST00000531380.1:c.1180C>A (FZD4) ENSP00000434034.1:p.Pro394Thr
ENST00000531521.1:n.747G>T (PRSS23)
ENST00000532234.5:c.*569G>T (PRSS23) ENSP00000436676.1:n.*569G>T
ENST00000533902.2:c.*291G>T (PRSS23) ENSP00000437268.1:n.*291G>T
NM_012193.3:c.1180C>A (FZD4) NP_036325.2:p.Pro394Thr
NR_120591.1:n.1241G>T (PRSS23)
NR_120592.1:n.990G>T (PRSS23)
NR_120591.2:n.939G>T (PRSS23)
NR_120592.2:n.688G>T (PRSS23)
NM_012193.4:c.1180C>A (FZD4) MANE Select NP_036325.2:p.Pro394Thr
NR_120591.3:n.939G>T (PRSS23)