Canonical Allele Identifier: CA2317263441
Gene: PRSS57 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.694649C= , CM000681.2:g.694649C= GRCh38
NC_000019.9:g.694649C= , CM000681.1:g.694649C= GRCh37
NC_000019.8:g.645649C= NCBI36
NG_051189.1:g.5883G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000329267.9:c.233+165G= MANE Select ENSP00000327386.6:n.233+165G=
ENST00000329267.8:c.233+165G= ENSP00000327386.6:n.233+165G=
ENST00000613411.4:c.236+165G= ENSP00000482358.1:n.236+165G=
NM_001308209.1:c.233+165G= NP_001295138.1:n.233+165G=
NM_214710.3:c.236+165G= NP_999875.1:n.236+165G=
NM_214710.4:c.236+165G= NP_999875.1:n.236+165G=
NM_001308209.2:c.233+165G= MANE Select NP_001295138.2:n.233+165G=
NM_214710.5:c.236+165G= NP_999875.2:n.236+165G=
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