Canonical Allele Identifier: CA402894378
Gene: PRSS57 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.694824A>T , CM000681.2:g.694824A>T GRCh38
NC_000019.9:g.694824A>T , CM000681.1:g.694824A>T GRCh37
NC_000019.8:g.645824A>T NCBI36
NG_051189.1:g.5708T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000329267.9:c.223T>A MANE Select ENSP00000327386.6:p.Phe75Ile
ENST00000329267.8:c.223T>A ENSP00000327386.6:p.Phe75Ile
ENST00000613411.4:c.226T>A ENSP00000482358.1:p.Phe76Ile
NM_001308209.1:c.223T>A NP_001295138.1:p.Phe75Ile
NM_214710.3:c.226T>A NP_999875.1:p.Phe76Ile
NM_214710.4:c.226T>A NP_999875.1:p.Phe76Ile
NM_001308209.2:c.223T>A MANE Select NP_001295138.2:p.Phe75Ile
NM_214710.5:c.226T>A NP_999875.2:p.Phe76Ile