Canonical Allele Identifier: CA2587779619
Gene: PRSS57 HGNC NCBI

Linked Data

gnomAD v4: 19-695292-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.695292T>A , CM000681.2:g.695292T>A GRCh38
NC_000019.9:g.695292T>A , CM000681.1:g.695292T>A GRCh37
NC_000019.8:g.646292T>A NCBI36
NG_051189.1:g.5240A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000329267.9:c.79+60A>T MANE Select ENSP00000327386.6:n.79+60A>T
ENST00000329267.8:c.79+60A>T ENSP00000327386.6:n.79+60A>T
ENST00000613411.4:c.79+60A>T ENSP00000482358.1:n.79+60A>T
NM_001308209.1:c.79+60A>T NP_001295138.1:n.79+60A>T
NM_214710.3:c.79+60A>T NP_999875.1:n.79+60A>T
NM_214710.4:c.79+60A>T NP_999875.1:n.79+60A>T
NM_001308209.2:c.79+60A>T MANE Select NP_001295138.2:n.79+60A>T
NM_214710.5:c.79+60A>T NP_999875.2:n.79+60A>T
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Search 100 bp 3'