Canonical Allele Identifier: CA2317263724
Gene: PRSS57 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.695222C= , CM000681.2:g.695222C= GRCh38
NC_000019.9:g.695222C= , CM000681.1:g.695222C= GRCh37
NC_000019.8:g.646222C= NCBI36
NG_051189.1:g.5310G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000329267.9:c.79+130G= MANE Select ENSP00000327386.6:n.79+130G=
ENST00000329267.8:c.79+130G= ENSP00000327386.6:n.79+130G=
ENST00000613411.4:c.79+130G= ENSP00000482358.1:n.79+130G=
NM_001308209.1:c.79+130G= NP_001295138.1:n.79+130G=
NM_214710.3:c.79+130G= NP_999875.1:n.79+130G=
NM_214710.4:c.79+130G= NP_999875.1:n.79+130G=
NM_001308209.2:c.79+130G= MANE Select NP_001295138.2:n.79+130G=
NM_214710.5:c.79+130G= NP_999875.2:n.79+130G=
Search 100 bp 5'
Search 100 bp 3'