Canonical Allele Identifier: CA504688273
Gene: PRSS57 HGNC NCBI

Linked Data

gnomAD v4: 19-694894-G-T
MyVariant Identifiers: chr19:g.694894G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.694894G>T , CM000681.2:g.694894G>T GRCh38
NC_000019.9:g.694894G>T , CM000681.1:g.694894G>T GRCh37
NC_000019.8:g.645894G>T NCBI36
NG_051189.1:g.5638C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000329267.9:c.153C>A MANE Select ENSP00000327386.6:p.Arg51=
ENST00000329267.8:c.153C>A ENSP00000327386.6:p.Arg51=
ENST00000613411.4:c.156C>A ENSP00000482358.1:p.Arg52=
NM_001308209.1:c.153C>A NP_001295138.1:p.Arg51=
NM_214710.3:c.156C>A NP_999875.1:p.Arg52=
NM_214710.4:c.156C>A NP_999875.1:p.Arg52=
NM_001308209.2:c.153C>A MANE Select NP_001295138.2:p.Arg51=
NM_214710.5:c.156C>A NP_999875.2:p.Arg52=
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