Canonical Allele Identifier: CA2317263686
Gene: PRSS57 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.695155C= , CM000681.2:g.695155C= GRCh38
NC_000019.9:g.695155C= , CM000681.1:g.695155C= GRCh37
NC_000019.8:g.646155C= NCBI36
NG_051189.1:g.5377G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000329267.9:c.80-188G= MANE Select ENSP00000327386.6:n.80-188G=
ENST00000329267.8:c.80-188G= ENSP00000327386.6:n.80-188G=
ENST00000613411.4:c.80-185G= ENSP00000482358.1:n.80-185G=
NM_001308209.1:c.80-188G= NP_001295138.1:n.80-188G=
NM_214710.3:c.80-185G= NP_999875.1:n.80-185G=
NM_214710.4:c.80-185G= NP_999875.1:n.80-185G=
NM_001308209.2:c.80-188G= MANE Select NP_001295138.2:n.80-188G=
NM_214710.5:c.80-185G= NP_999875.2:n.80-185G=
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