Canonical Allele Identifier: CA2317263717
Gene: PRSS57 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.695201A= , CM000681.2:g.695201A= GRCh38
NC_000019.9:g.695201A= , CM000681.1:g.695201A= GRCh37
NC_000019.8:g.646201A= NCBI36
NG_051189.1:g.5331T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000329267.9:c.79+151T= MANE Select ENSP00000327386.6:n.79+151T=
ENST00000329267.8:c.79+151T= ENSP00000327386.6:n.79+151T=
ENST00000613411.4:c.79+151T= ENSP00000482358.1:n.79+151T=
NM_001308209.1:c.79+151T= NP_001295138.1:n.79+151T=
NM_214710.3:c.79+151T= NP_999875.1:n.79+151T=
NM_214710.4:c.79+151T= NP_999875.1:n.79+151T=
NM_001308209.2:c.79+151T= MANE Select NP_001295138.2:n.79+151T=
NM_214710.5:c.79+151T= NP_999875.2:n.79+151T=
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