Canonical Allele Identifier: CA402894520

Gene: PRSS57

Linked Data

• MyVariant Identifiers: chr19:g.694866A>T (hg19) ; chr19:g.694866A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.694866A>T , CM000681.2:g.694866A>T	GRCh38
NC_000019.9:g.694866A>T , CM000681.1:g.694866A>T	GRCh37
NC_000019.8:g.645866A>T	NCBI36
NG_051189.1:g.5666T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329267.9:c.181T>A MANE Select	ENSP00000327386.6:p.Phe61Ile
ENST00000329267.8:c.181T>A	ENSP00000327386.6:p.Phe61Ile
ENST00000613411.4:c.184T>A	ENSP00000482358.1:p.Phe62Ile
NM_001308209.1:c.181T>A	NP_001295138.1:p.Phe61Ile
NM_214710.3:c.184T>A	NP_999875.1:p.Phe62Ile
NM_214710.4:c.184T>A	NP_999875.1:p.Phe62Ile
NM_001308209.2:c.181T>A MANE Select	NP_001295138.2:p.Phe61Ile
NM_214710.5:c.184T>A	NP_999875.2:p.Phe62Ile