Canonical Allele Identifier: CA2813227830

Gene: PRSS57

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.694961dup , CM000681.2:g.694961dup	GRCh38
NC_000019.9:g.694961dup , CM000681.1:g.694961dup	GRCh37
NC_000019.8:g.645961dup	NCBI36
NG_051189.1:g.5576dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329267.9:c.91dup MANE Select	ENSP00000327386.6:p.Ala31GlyfsTer?
ENST00000329267.8:c.91dup	ENSP00000327386.6:p.Ala31GlyfsTer?
ENST00000613411.4:c.94dup	ENSP00000482358.1:p.Ala32GlyfsTer?
NM_001308209.1:c.91dup	NP_001295138.1:p.Ala31GlyfsTer?
NM_214710.3:c.94dup	NP_999875.1:p.Ala32GlyfsTer?
NM_214710.4:c.94dup	NP_999875.1:p.Ala32GlyfsTer?
NM_001308209.2:c.91dup MANE Select	NP_001295138.2:p.Ala31GlyfsTer?
NM_214710.5:c.94dup	NP_999875.2:p.Ala32GlyfsTer?