Canonical Allele Identifier: CA402894743
Gene: PRSS57 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.694937T>C , CM000681.2:g.694937T>C GRCh38
NC_000019.9:g.694937T>C , CM000681.1:g.694937T>C GRCh37
NC_000019.8:g.645937T>C NCBI36
NG_051189.1:g.5595A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000329267.9:c.110A>G MANE Select ENSP00000327386.6:p.His37Arg
ENST00000329267.8:c.110A>G ENSP00000327386.6:p.His37Arg
ENST00000613411.4:c.113A>G ENSP00000482358.1:p.His38Arg
NM_001308209.1:c.110A>G NP_001295138.1:p.His37Arg
NM_214710.3:c.113A>G NP_999875.1:p.His38Arg
NM_214710.4:c.113A>G NP_999875.1:p.His38Arg
NM_001308209.2:c.110A>G MANE Select NP_001295138.2:p.His37Arg
NM_214710.5:c.113A>G NP_999875.2:p.His38Arg