Canonical Allele Identifier: CA402894550

Gene: PRSS57

Linked Data

• MyVariant Identifiers: chr19:g.694875A>T (hg19) ; chr19:g.694875A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.694875A>T , CM000681.2:g.694875A>T	GRCh38
NC_000019.9:g.694875A>T , CM000681.1:g.694875A>T	GRCh37
NC_000019.8:g.645875A>T	NCBI36
NG_051189.1:g.5657T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329267.9:c.172T>A MANE Select	ENSP00000327386.6:p.Cys58Ser
ENST00000329267.8:c.172T>A	ENSP00000327386.6:p.Cys58Ser
ENST00000613411.4:c.175T>A	ENSP00000482358.1:p.Cys59Ser
NM_001308209.1:c.172T>A	NP_001295138.1:p.Cys58Ser
NM_214710.3:c.175T>A	NP_999875.1:p.Cys59Ser
NM_214710.4:c.175T>A	NP_999875.1:p.Cys59Ser
NM_001308209.2:c.172T>A MANE Select	NP_001295138.2:p.Cys58Ser
NM_214710.5:c.175T>A	NP_999875.2:p.Cys59Ser