Canonical Allele Identifier: CA504688221
Gene: PRSS57 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.694858C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.694858C>G , CM000681.2:g.694858C>G GRCh38
NC_000019.9:g.694858C>G , CM000681.1:g.694858C>G GRCh37
NC_000019.8:g.645858C>G NCBI36
NG_051189.1:g.5674G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000329267.9:c.189G>C MANE Select ENSP00000327386.6:p.Leu63=
ENST00000329267.8:c.189G>C ENSP00000327386.6:p.Leu63=
ENST00000613411.4:c.192G>C ENSP00000482358.1:p.Leu64=
NM_001308209.1:c.189G>C NP_001295138.1:p.Leu63=
NM_214710.3:c.192G>C NP_999875.1:p.Leu64=
NM_214710.4:c.192G>C NP_999875.1:p.Leu64=
NM_001308209.2:c.189G>C MANE Select NP_001295138.2:p.Leu63=
NM_214710.5:c.192G>C NP_999875.2:p.Leu64=